NO116080B - - Google Patents
Info
- Publication number
- NO116080B NO116080B NO168038A NO16803867A NO116080B NO 116080 B NO116080 B NO 116080B NO 168038 A NO168038 A NO 168038A NO 16803867 A NO16803867 A NO 16803867A NO 116080 B NO116080 B NO 116080B
- Authority
- NO
- Norway
- Prior art keywords
- formaldehyde
- groups
- water
- dithiols
- temperature
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 41
- 150000004662 dithiols Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 4
- 229920006295 polythiol Polymers 0.000 claims description 3
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000000047 product Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000000203 mixture Substances 0.000 description 10
- 235000019256 formaldehyde Nutrition 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 150000002009 diols Chemical class 0.000 description 4
- INBDPOJZYZJUDA-UHFFFAOYSA-N methanedithiol Chemical compound SCS INBDPOJZYZJUDA-UHFFFAOYSA-N 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000008098 formaldehyde solution Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 239000012264 purified product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000219492 Quercus Species 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000009950 felting Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- -1 monothioether polyols Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR60811A FR1487364A (fr) | 1966-05-09 | 1966-05-09 | Procédé de préparation de glycols polythioéthers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO116080B true NO116080B (da) | 1969-01-27 |
Family
ID=8608155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO168038A NO116080B (da) | 1966-05-09 | 1967-05-08 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3519689A (da) |
| AT (1) | AT269822B (da) |
| BE (1) | BE698147A (da) |
| CH (1) | CH472394A (da) |
| DE (1) | DE1618892B1 (da) |
| DK (1) | DK120336B (da) |
| ES (1) | ES340143A1 (da) |
| FR (1) | FR1487364A (da) |
| GB (1) | GB1177827A (da) |
| LU (1) | LU53605A1 (da) |
| NL (1) | NL6706189A (da) |
| NO (1) | NO116080B (da) |
| OA (1) | OA02426A (da) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3962186A (en) * | 1973-08-16 | 1976-06-08 | The Dow Chemical Company | Curable composition of a polyepoxide with a methylol derivative of a polythiol |
| US3968167A (en) * | 1975-02-07 | 1976-07-06 | The Dow Chemical Company | Methylol derivatives of polythiols |
| ATE5535T1 (de) * | 1981-02-05 | 1983-12-15 | Sandoz Ag | Bis- und poly-disulfide mit immunostimulierender aktivitaet. |
| IT1174495B (it) * | 1984-02-17 | 1987-07-01 | Nuovo Consoricio Sanitario Nat | Composti ad attivita'ipolipemizzante |
| US5801290A (en) * | 1994-01-11 | 1998-09-01 | Arco Chemical Technology, L.P. | Process for making poly(thioether ether)s from diallyl ether and dithiols |
| CN111909365B (zh) * | 2019-05-09 | 2022-09-20 | 江汉大学 | 一种硫醚聚酯的制备方法 |
-
1966
- 1966-05-09 FR FR60811A patent/FR1487364A/fr not_active Expired
-
1967
- 1967-05-02 GB GB20366/67A patent/GB1177827A/en not_active Expired
- 1967-05-03 NL NL6706189A patent/NL6706189A/xx unknown
- 1967-05-03 CH CH630567A patent/CH472394A/fr not_active IP Right Cessation
- 1967-05-03 DK DK233967AA patent/DK120336B/da unknown
- 1967-05-05 ES ES340143A patent/ES340143A1/es not_active Expired
- 1967-05-05 AT AT423667A patent/AT269822B/de active
- 1967-05-05 LU LU53605D patent/LU53605A1/xx unknown
- 1967-05-05 OA OA52924A patent/OA02426A/xx unknown
- 1967-05-05 DE DE1967S0109746 patent/DE1618892B1/de active Pending
- 1967-05-08 NO NO168038A patent/NO116080B/no unknown
- 1967-05-08 US US636652A patent/US3519689A/en not_active Expired - Lifetime
- 1967-05-08 BE BE698147D patent/BE698147A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES340143A1 (es) | 1968-09-01 |
| NL6706189A (da) | 1967-11-10 |
| DK120336B (da) | 1971-05-17 |
| GB1177827A (en) | 1970-01-14 |
| FR1487364A (fr) | 1967-07-07 |
| DE1618892B1 (de) | 1972-01-05 |
| CH472394A (fr) | 1969-05-15 |
| BE698147A (da) | 1967-11-18 |
| OA02426A (fr) | 1970-05-05 |
| LU53605A1 (da) | 1968-02-12 |
| AT269822B (de) | 1969-04-10 |
| US3519689A (en) | 1970-07-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO168038B (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive 7-oksabicykloheptan-substituerte diamider og deres kongenere prostaglandinanaloger. | |
| NO116080B (da) | ||
| US2467212A (en) | Liquid urea-formaldehyde compositions | |
| Erdtman et al. | Aromatic keto-and hydroxy-polyethers as lignin models. II | |
| US2228159A (en) | Manufacture of cation-exchanging bodies | |
| US2372602A (en) | Process for preparation of pentaerythritol | |
| US2325589A (en) | Acetaldehyde-formaldehyde condensation product | |
| US2095320A (en) | Manufacture of cyclic ddzihers | |
| US2754335A (en) | Triphenylols | |
| US3004006A (en) | Omega-hydroxypolyoxyalkyleneoxybenzene sulfonates | |
| USRE23174E (en) | Liquid urea-formaldehyde | |
| Fenton et al. | LVI.—Crystalline glycollic aldehyde | |
| US2894971A (en) | Polyfluoroalkyl p-toluenesulfonates | |
| RU2441038C2 (ru) | Способ получения полисульфидов, полисульфиды и их применение | |
| US2572256A (en) | Transparent urea-aldehyde type resins and method for producing the same | |
| Korshak et al. | Synthesis and properties of polycondensation polymers from compounds with asymmetric functional groups | |
| JPH01318040A (ja) | 芳香族ポリエーテルスルホン | |
| US2783216A (en) | Resinous products from mannich bases of aromatic polyketones with hydrogen sulfide andor polythiols | |
| US3240764A (en) | Polythiosemicarbazide chelates | |
| US2612526A (en) | Pentaerythritol manufacture | |
| US2186272A (en) | Process for the preparation of pentaerythritol | |
| Hayashi | Reactions of 2, 2'-Dithiobis (2-methylpropionaldehyde) | |
| US2181476A (en) | Aliphatic hydroxy-ether ketones | |
| US3121709A (en) | Resinous reaction products derived from lignins | |
| US2756237A (en) | Polyalkanol pyridines and process of making them |