NO132189B - - Google Patents

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Info

Publication number: NO132189B
Authority: NO; Norway
Prior art keywords: dione; methyl; pregnadiene; compound; triol
Prior art date: 1968-09-09

Application number

NO3519/69A

Other languages

English (en)

Norwegian (no)

Other versions

NO132189C (sv

Inventor

L J Marshall

Original Assignee

Redland Tiles Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1968-09-09

Filing date

1969-09-02

Publication date

1975-06-23

1969-09-02 Application filed by Redland Tiles Ltd filed Critical Redland Tiles Ltd

1975-06-23 Publication of NO132189B publication Critical patent/NO132189B/no

1975-10-01 Publication of NO132189C publication Critical patent/NO132189C/no

Links

150000001875 compounds Chemical class 0.000 claims description 26
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 20
238000000034 method Methods 0.000 claims description 15
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 claims description 14
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 14
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 7
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 5
239000012359 Methanesulfonyl chloride Substances 0.000 claims description 5
239000002253 acid Substances 0.000 claims description 5
QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 claims description 5
239000012024 dehydrating agents‎ Substances 0.000 claims description 4
229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 4
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims description 4
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 claims description 3
DKSMCEUSSQTGBK-UHFFFAOYSA-N bromous acid Chemical compound OBr=O DKSMCEUSSQTGBK-UHFFFAOYSA-N 0.000 claims description 3
238000011065 in-situ storage Methods 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
239000000126 substance Substances 0.000 claims description 2
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 36
239000000203 mixture Substances 0.000 description 29
239000000243 solution Substances 0.000 description 24
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 22
238000006243 chemical reaction Methods 0.000 description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 16
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 13
-1 triene compound Chemical class 0.000 description 12
238000001914 filtration Methods 0.000 description 11
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
239000011541 reaction mixture Substances 0.000 description 9
238000002360 preparation method Methods 0.000 description 8
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
239000002904 solvent Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000003513 alkali Substances 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
239000007858 starting material Substances 0.000 description 6
230000007306 turnover Effects 0.000 description 6
229960000583 acetic acid Drugs 0.000 description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
230000007062 hydrolysis Effects 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
239000000725 suspension Substances 0.000 description 4
239000002585 base Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
230000018044 dehydration Effects 0.000 description 3
238000006297 dehydration reaction Methods 0.000 description 3
150000003944 halohydrins Chemical class 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
239000000047 product Substances 0.000 description 3
238000003756 stirring Methods 0.000 description 3
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
239000004215 Carbon black (E152) Substances 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
230000003110 anti-inflammatory effect Effects 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
239000012362 glacial acetic acid Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
239000010410 layer Substances 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
229910000027 potassium carbonate Inorganic materials 0.000 description 2
JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
229940014800 succinic anhydride Drugs 0.000 description 2
JAUFWTSSYRTLLB-UHFFFAOYSA-N (2-phenylacetyl) 2-phenylacetate Chemical compound C=1C=CC=CC=1CC(=O)OC(=O)CC1=CC=CC=C1 JAUFWTSSYRTLLB-UHFFFAOYSA-N 0.000 description 1
ODIGIKRIUKFKHP-UHFFFAOYSA-N (n-propan-2-yloxycarbonylanilino) acetate Chemical compound CC(C)OC(=O)N(OC(C)=O)C1=CC=CC=C1 ODIGIKRIUKFKHP-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
FUFLCEKSBBHCMO-UHFFFAOYSA-N 11-dehydrocorticosterone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)C(=O)CO)C4C3CCC2=C1 FUFLCEKSBBHCMO-UHFFFAOYSA-N 0.000 description 1
NOGFHTGYPKWWRX-UHFFFAOYSA-N 2,2,6,6-tetramethyloxan-4-one Chemical compound CC1(C)CC(=O)CC(C)(C)O1 NOGFHTGYPKWWRX-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
MFYSYFVPBJMHGN-ZPOLXVRWSA-N Cortisone Chemical compound O=C1CC[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 MFYSYFVPBJMHGN-ZPOLXVRWSA-N 0.000 description 1
MFYSYFVPBJMHGN-UHFFFAOYSA-N Cortisone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)(O)C(=O)CO)C4C3CCC2=C1 MFYSYFVPBJMHGN-UHFFFAOYSA-N 0.000 description 1
YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
208000029422 Hypernatremia Diseases 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
SNAYLCYCEXREJX-WWSDEZETSA-N [(3r,8s,9s,10s,13s,14s)-17-acetyl-10,13,16-trimethyl-11-oxo-1,2,3,4,5,6,7,8,9,12,14,15-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate Chemical compound C1C(=O)[C@@H]2[C@@]3(C)CC[C@@H](OC(=O)C)CC3CC[C@H]2[C@@H]2CC(C)=C(C(C)=O)[C@]21C SNAYLCYCEXREJX-WWSDEZETSA-N 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
OWAQXCQNWNJICI-UHFFFAOYSA-N benzene;chloroform Chemical compound ClC(Cl)Cl.C1=CC=CC=C1 OWAQXCQNWNJICI-UHFFFAOYSA-N 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
230000031709 bromination Effects 0.000 description 1
238000005893 bromination reaction Methods 0.000 description 1
VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
DQSHRNZTQWDMPJ-UHFFFAOYSA-N chlorosulfinyloxymethane Chemical compound COS(Cl)=O DQSHRNZTQWDMPJ-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
229960004544 cortisone Drugs 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000010828 elution Methods 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
230000001976 improved effect Effects 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000006140 methanolysis reaction Methods 0.000 description 1
VBTQNRFWXBXZQR-UHFFFAOYSA-N n-bromoacetamide Chemical compound CC(=O)NBr VBTQNRFWXBXZQR-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
229960003424 phenylacetic acid Drugs 0.000 description 1
239000003279 phenylacetic acid Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
235000011056 potassium acetate Nutrition 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
229940107700 pyruvic acid Drugs 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
206010039073 rheumatoid arthritis Diseases 0.000 description 1
DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
229910000033 sodium borohydride Inorganic materials 0.000 description 1
239000012279 sodium borohydride Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65G—TRANSPORT OR STORAGE DEVICES, e.g. CONVEYORS FOR LOADING OR TIPPING, SHOP CONVEYOR SYSTEMS OR PNEUMATIC TUBE CONVEYORS
- B65G47/00—Article or material-handling devices associated with conveyors; Methods employing such devices
- B65G47/52—Devices for transferring articles or materials between conveyors i.e. discharging or feeding devices
- B65G47/68—Devices for transferring articles or materials between conveyors i.e. discharging or feeding devices adapted to receive articles arriving in one layer from one conveyor lane and to transfer them in individual layers to more than one conveyor lane or to one broader conveyor lane, or vice versa, e.g. combining the flows of articles conveyed by more than one conveyor
- B65G47/71—Devices for transferring articles or materials between conveyors i.e. discharging or feeding devices adapted to receive articles arriving in one layer from one conveyor lane and to transfer them in individual layers to more than one conveyor lane or to one broader conveyor lane, or vice versa, e.g. combining the flows of articles conveyed by more than one conveyor the articles being discharged or distributed to several distinct separate conveyors or to a broader conveyor lane
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65G—TRANSPORT OR STORAGE DEVICES, e.g. CONVEYORS FOR LOADING OR TIPPING, SHOP CONVEYOR SYSTEMS OR PNEUMATIC TUBE CONVEYORS
- B65G37/00—Combinations of mechanical conveyors of the same kind, or of different kinds, of interest apart from their application in particular machines or use in particular manufacturing processes
- B65G37/005—Combinations of mechanical conveyors of the same kind, or of different kinds, of interest apart from their application in particular machines or use in particular manufacturing processes comprising two or more co-operating conveying elements with parallel longitudinal axes

Landscapes

Engineering & Computer Science (AREA)
Mechanical Engineering (AREA)
Intermediate Stations On Conveyors (AREA)
Devices For Post-Treatments, Processing, Supply, Discharge, And Other Processes (AREA)
Warehouses Or Storage Devices (AREA)
Branching, Merging, And Special Transfer Between Conveyors (AREA)
Steroid Compounds (AREA)
Processing Of Stones Or Stones Resemblance Materials (AREA)

NO3519/69A 1968-09-09 1969-09-02 NO132189C (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB42883/68A GB1286803A (en)	1968-09-09	1968-09-09	Improvements in or relating to the manufacture of roofing tiles

Publications (2)

Publication Number	Publication Date
NO132189B true NO132189B (sv)	1975-06-23
NO132189C NO132189C (sv)	1975-10-01

Family

ID=10426380

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO3519/69A NO132189C (sv)	1968-09-09	1969-09-02

Country Status (15)

Country	Link
US (1)	US3604552A (sv)
JP (1)	JPS491830B1 (sv)
AT (1)	AT302871B (sv)
BE (1)	BE738536A (sv)
CH (1)	CH504370A (sv)
CS (1)	CS152329B2 (sv)
DE (1)	DE1945416C3 (sv)
ES (1)	ES371299A1 (sv)
FR (1)	FR2017659A1 (sv)
GB (1)	GB1286803A (sv)
NL (1)	NL154140B (sv)
NO (1)	NO132189C (sv)
SE (1)	SE354984B (sv)
SU (1)	SU386499A3 (sv)
ZA (1)	ZA696082B (sv)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1391320B1 (it) *	2008-10-29	2011-12-05	Azionaria Costruzioni Acma Spa	Dispositivo di suddivisione in almeno due file di prodotti alimentati secondo una fila.
CN113247641B (zh) *	2021-06-30	2022-11-11	江苏中轩建设有限公司	一种方砖垛辅助卸砖装置
CN114074831B (zh) *	2022-01-20	2022-06-03	百信信息技术有限公司	一种组装生产线

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH159006A (de) *	1930-12-05	1932-12-15	Walder & Co	Förderanlage für fliessenden Transport in Schuhfabriken.
DE845922C (de) *	1944-06-30	1952-08-07	Buderus Eisenwerk	Verfahren und Vorrichtung zum Foerdern mittels geneigter Bahnen, z. B. Schienen od. dgl.
US2581599A (en) *	1946-12-10	1952-01-08	Coe Mfg Co	Sheet handling apparatus
US2884115A (en) *	1955-03-29	1959-04-28	Baker Perkins Ltd	Manufacture of biscuits
FR1239045A (fr) *	1958-10-15	1960-08-19	Redland Tiles Ltd	Installation à transporteur convoyeur
DE1158445B (de) *	1958-10-15	1963-11-28	Redland Tiles Ltd	Be- und Entladevorrichtung fuer insbesondere mit Ziegeln zu beladende Traggestelle
DE1201969B (de) *	1960-06-30	1965-09-30	Ruhenstroth G M B H W	Beschickvorrichtung fuer einen be- und entladene Beschickbleche aufnehmenden Beschickkorb zu Etagenpressen beispielsweise fuer die Herstellung von Furnierplatten
FR1384999A (fr) *	1964-02-06	1965-01-08		Installation automatique pour le chargement ordonné d'éléments sur des châssis ou analogues
AT254014B (de) *	1964-02-14	1967-05-10	Enrico Putin	Vorrichtung zum gleichzeitigen Be- und Entladen ein- oder mehrflächiger Gestelle
US3416640A (en) *	1965-02-24	1968-12-17	Svobida Loren	Automatic divider
US3348655A (en) *	1966-12-06	1967-10-24	Kliklok Corp	Device for disentangling and conveying flanged receptacles

1968
- 1968-09-09 GB GB42883/68A patent/GB1286803A/en not_active Expired
1969
- 1969-08-25 ZA ZA696082*A patent/ZA696082B/xx unknown
- 1969-08-26 US US853109A patent/US3604552A/en not_active Expired - Lifetime
- 1969-09-02 NO NO3519/69A patent/NO132189C/no unknown
- 1969-09-02 NL NL696913364A patent/NL154140B/xx not_active IP Right Cessation
- 1969-09-08 JP JP44071184A patent/JPS491830B1/ja active Pending
- 1969-09-08 CS CS6124A patent/CS152329B2/cs unknown
- 1969-09-08 CH CH1357969A patent/CH504370A/de not_active IP Right Cessation
- 1969-09-08 SU SU1360705A patent/SU386499A3/ru active
- 1969-09-08 DE DE1945416A patent/DE1945416C3/de not_active Expired
- 1969-09-08 SE SE12364/69A patent/SE354984B/xx unknown
- 1969-09-08 ES ES371299A patent/ES371299A1/es not_active Expired
- 1969-09-08 AT AT851669A patent/AT302871B/de not_active IP Right Cessation
- 1969-09-08 BE BE738536D patent/BE738536A/xx not_active IP Right Cessation
- 1969-09-09 FR FR6930589A patent/FR2017659A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
DE1945416B2 (de)	1980-10-30
FR2017659A1 (sv)	1970-05-22
GB1286803A (en)	1972-08-23
DE1945416C3 (de)	1981-06-11
CS152329B2 (sv)	1973-12-19
DE1945419A1 (de)	1970-10-01
JPS491830B1 (sv)	1974-01-17
NL6913364A (sv)	1970-03-11
SU386499A3 (sv)	1973-06-14
NO132189C (sv)	1975-10-01
AT302871B (de)	1972-10-25
CH504370A (de)	1971-03-15
DE1945405B2 (de)	1975-10-09
NL154140B (nl)	1977-08-15
ES371299A1 (es)	1971-09-01
US3604552A (en)	1971-09-14
SE354984B (sv)	1973-04-02
DE1945419B2 (de)	1975-10-09
DE1945405A1 (de)	1970-08-06
ZA696082B (en)	1971-04-28
BE738536A (sv)	1970-03-09
DE1945416A1 (de)	1970-09-17

Publication	Publication Date	Title
US2763671A (en)	1956-09-18	9alpha, 21-dihalopregnanes and process
NO162506B (no)	1989-10-02	Anordning for loefte fisk.
US3839369A (en)	1974-10-01	Process for the production of delta4,9(11),16-3,20-diketo steroids
US2781366A (en)	1957-02-12	11beta, 21-dihydroxy-4, 16, 20-pregnatriene-3-one and esters thereof
US3842105A (en)	1974-10-15	Process for the preparation of 16,17-unsaturated steroids
US2777843A (en)	1957-01-15	Preparation of 4-pregnen-17alpha-ol-3, 20-dione
US2786857A (en)	1957-03-26	Process for producing 17-hydroxy-desoxycorticosterone
NO132189B (sv)	1975-06-23
JPS6052160B2 (ja)	1985-11-18	プレグナン系のｄ−ホモステロイドの製造方法
US2769823A (en)	1956-11-06	Preparation of 17alpha-hydroxy-20-keto-pregnenes
US2884417A (en)	1959-04-28	5, 6-dichloro pregnanes
US2786837A (en)	1957-03-26	Compounds for synthesizing steroids
US2916486A (en)	1959-12-08	6-fluoro steroids and intermediates therefor
US2832773A (en)	1958-04-29	Diazo-ketones for synthesizing steroids
US3947409A (en)	1976-03-30	16-Alkyl-1,4,9(11)-pregnatrienes and 9,11-epoxides thereof
US3795687A (en)	1974-03-05	Process for the production of 6-fluoro-5-bromo-13-ethyl steroids
US3684800A (en)	1972-08-15	Di-epoxide process for the preparation of 9{60 -fluoro-16-methylene-prednisolone or-prednisone, and 21-esters thereof
US3047596A (en)	1962-07-31	6alpha-halogen-9alpha-halogen-delta-pregnadiene-3-one compounds
US2751401A (en)	1956-06-19	4-chloropregnane-17alpha, 21-diol-3, 11, 20-trione and 21-esters thereof
US3009932A (en)	1961-11-21	6-fluoro-9alpha, 11beta- 21-trihalo-progesterones
US3767685A (en)	1973-10-23	Novel 11beta-halo-steroids of the oestrane series
DE1668658A1 (de)	1971-04-15	Herstellung von neuen Halogen-Steroiden
NO132391B (sv)	1975-07-28
US2953581A (en)	1960-09-20	3-oxygenated-20-keto-21-fluoro-pregnanes
US2833790A (en)	1958-05-06	5-halo-17(20)-bisnorcholenal compounds and process for preparing same