NO782285L - Reduksjon av fosfinoksyder. - Google Patents

Reduksjon av fosfinoksyder.

Info

Publication number: NO782285L
Authority: NO; Norway
Prior art keywords: amine; stated; phosphine oxide; oxide; phosphine
Prior art date: 1977-07-05

Application number

NO782285A

Other languages

English (en)

Norwegian (no)

Inventor

William Robert Davis

Michael David Gordon

Original Assignee

M & T Chemicals Inc

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.)

1977-07-05

Filing date

1978-06-30

Publication date

1979-01-08

1978-06-30 Application filed by M & T Chemicals Inc filed Critical M & T Chemicals Inc

1979-01-08 Publication of NO782285L publication Critical patent/NO782285L/no

Links

XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 title claims description 14
229910000073 phosphorus hydride Inorganic materials 0.000 title claims description 7
150000001412 amines Chemical class 0.000 claims description 19
238000000034 method Methods 0.000 claims description 16
AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical group P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims description 14
238000006243 chemical reaction Methods 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
150000003377 silicon compounds Chemical class 0.000 claims description 5
FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical group C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 claims description 5
ZDHXKXAHOVTTAH-UHFFFAOYSA-N trichlorosilane Chemical group Cl[SiH](Cl)Cl ZDHXKXAHOVTTAH-UHFFFAOYSA-N 0.000 claims description 4
239000005052 trichlorosilane Substances 0.000 claims description 4
150000003335 secondary amines Chemical class 0.000 claims description 3
150000003141 primary amines Chemical class 0.000 claims 2
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
229910000077 silane Inorganic materials 0.000 description 7
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 6
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 6
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
150000002430 hydrocarbons Chemical group 0.000 description 4
-1 keto- Chemical class 0.000 description 4
239000012074 organic phase Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
238000004821 distillation Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 3
239000000047 product Substances 0.000 description 3
150000004756 silanes Chemical class 0.000 description 3
235000011121 sodium hydroxide Nutrition 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000004793 Polystyrene Substances 0.000 description 2
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000003513 alkali Substances 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
125000003368 amide group Chemical group 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
239000005046 Chlorosilane Substances 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
229910000272 alkali metal oxide Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
238000010533 azeotropic distillation Methods 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
FSUCAIIDBUYEFT-UHFFFAOYSA-N dichloro(ethoxy)silane Chemical compound CCO[SiH](Cl)Cl FSUCAIIDBUYEFT-UHFFFAOYSA-N 0.000 description 1
XNAFLNBULDHNJS-UHFFFAOYSA-N dichloro(phenyl)silicon Chemical compound Cl[Si](Cl)C1=CC=CC=C1 XNAFLNBULDHNJS-UHFFFAOYSA-N 0.000 description 1
MROCJMGDEKINLD-UHFFFAOYSA-N dichlorosilane Chemical compound Cl[SiH2]Cl MROCJMGDEKINLD-UHFFFAOYSA-N 0.000 description 1
229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
239000001257 hydrogen Chemical group 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000010410 layer Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
125000004437 phosphorous atom Chemical group 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
238000003918 potentiometric titration Methods 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000010703 silicon Substances 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000011343 solid material Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Chemical group 0.000 description 1
MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/505—Preparation; Separation; Purification; Stabilisation
- C07F9/509—Preparation; Separation; Purification; Stabilisation by reduction of pentavalent phosphorus derivatives, e.g. -P=X with X = O, S, Se or -P-Hal2

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

NO782285A 1977-07-05 1978-06-30 Reduksjon av fosfinoksyder. NO782285L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/812,761 US4131624A (en)	1977-07-05	1977-07-05	Reduction of phosphine oxides

Publications (1)

Publication Number	Publication Date
NO782285L true NO782285L (no)	1979-01-08

Family

ID=25210549

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO782285A NO782285L (no)	1977-07-05	1978-06-30	Reduksjon av fosfinoksyder.

Country Status (22)

Country	Link
US (1)	US4131624A (fr)
JP (1)	JPS5414947A (fr)
AT (1)	AT356139B (fr)
AU (1)	AU515469B2 (fr)
BE (1)	BE868462A (fr)
BR (1)	BR7804225A (fr)
CA (1)	CA1088573A (fr)
DE (1)	DE2828604C2 (fr)
DK (1)	DK145379C (fr)
ES (1)	ES471408A1 (fr)
FR (1)	FR2396763A1 (fr)
GB (1)	GB2000780B (fr)
IL (1)	IL54925A (fr)
IT (1)	IT1161399B (fr)
NL (1)	NL7807243A (fr)
NO (1)	NO782285L (fr)
NZ (1)	NZ187700A (fr)
PL (1)	PL208160A1 (fr)
SE (1)	SE7807482L (fr)
SU (1)	SU710518A3 (fr)
YU (1)	YU154778A (fr)
ZA (1)	ZA783535B (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4507501A (en) *	1983-10-26	1985-03-26	Ethyl Corporation	Process for preparing tertiary phosphines
US4507502A (en) *	1983-10-26	1985-03-26	Ethyl Corporation	Process for preparing tertiary phosphines
US4507504A (en) *	1983-11-25	1985-03-26	Ethyl Corporation	Process for preparing tertiary phosphines
US4507503A (en) *	1983-11-25	1985-03-26	Ethyl Corporation	Process for preparing tertiary phosphines
US4514575A (en) *	1983-11-25	1985-04-30	Ethyl Corporation	Process for preparing tertiary phosphines
DE4142679A1 (de) *	1991-12-23	1993-07-01	Basf Ag	Verfahren zur herstellung von tertiaeren phosphinen
CN101270132B (zh) *	2007-11-08	2010-11-03	陈国君	用三苯基氧化膦生产三苯基膦的方法
US8901365B2 (en) *	2009-04-06	2014-12-02	Board Of Regents, The University Of Texas System	Catalytic Wittig and Mitsunobu reactions
CN106674278A (zh) *	2016-12-16	2017-05-17	浙江先锋科技股份有限公司	一种三苯基氧膦废渣中的三苯基膦回收工艺
WO2020077582A1 (fr) *	2018-10-18	2020-04-23	Rhodia Operations	Procédé de préparation de phosphines tertiaires
CN110343133A (zh) *	2019-07-03	2019-10-18	闫福全	一种还原法生产三苯基膦的方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1203773B (de) *	1964-05-16	1965-10-28	Shell Int Research	Verfahren zur Herstellung von tertiaeren Phosphinen
NL295914A (fr) *	1962-07-31
US4008282A (en) *	1973-12-14	1977-02-15	Hoffmann-La Roche Inc.	Preparation of triaryl phosphines

1977
- 1977-07-05 US US05/812,761 patent/US4131624A/en not_active Expired - Lifetime
1978
- 1978-06-15 IL IL54925A patent/IL54925A/xx unknown
- 1978-06-20 ZA ZA00783535A patent/ZA783535B/xx unknown
- 1978-06-22 GB GB7827585A patent/GB2000780B/en not_active Expired
- 1978-06-26 FR FR7818982A patent/FR2396763A1/fr not_active Withdrawn
- 1978-06-26 BE BE188847A patent/BE868462A/fr unknown
- 1978-06-27 NZ NZ187700A patent/NZ187700A/xx unknown
- 1978-06-29 AT AT473678A patent/AT356139B/de not_active IP Right Cessation
- 1978-06-29 DE DE2828604A patent/DE2828604C2/de not_active Expired
- 1978-06-29 YU YU01547/78A patent/YU154778A/xx unknown
- 1978-06-30 BR BR7804225A patent/BR7804225A/pt unknown
- 1978-06-30 NO NO782285A patent/NO782285L/no unknown
- 1978-06-30 AU AU37642/78A patent/AU515469B2/en not_active Expired
- 1978-07-03 SE SE7807482A patent/SE7807482L/xx unknown
- 1978-07-04 CA CA306,757A patent/CA1088573A/fr not_active Expired
- 1978-07-04 DK DK302578A patent/DK145379C/da active
- 1978-07-04 ES ES471408A patent/ES471408A1/es not_active Expired
- 1978-07-04 NL NL7807243A patent/NL7807243A/xx not_active Application Discontinuation
- 1978-07-04 PL PL20816078A patent/PL208160A1/xx unknown
- 1978-07-04 IT IT09520/78A patent/IT1161399B/it active
- 1978-07-04 SU SU782631648A patent/SU710518A3/ru active
- 1978-07-05 JP JP8103478A patent/JPS5414947A/ja active Pending

Also Published As

Publication number	Publication date
ATA473678A (de)	1979-09-15
PL208160A1 (pl)	1979-07-02
GB2000780B (en)	1982-01-27
JPS5414947A (en)	1979-02-03
US4131624A (en)	1978-12-26
IT1161399B (it)	1987-03-18
AU3764278A (en)	1980-01-03
BR7804225A (pt)	1979-03-13
GB2000780A (en)	1979-01-17
IL54925A (en)	1982-01-31
DK145379B (da)	1982-11-08
DK302578A (da)	1979-01-06
NL7807243A (nl)	1979-01-09
ZA783535B (en)	1979-06-27
DE2828604C2 (de)	1982-12-30
ES471408A1 (es)	1979-01-16
SU710518A3 (ru)	1980-01-15
DK145379C (da)	1983-04-11
SE7807482L (sv)	1979-01-06
YU154778A (en)	1983-01-21
AT356139B (de)	1980-04-10
FR2396763A1 (fr)	1979-02-02
NZ187700A (en)	1980-05-27
BE868462A (fr)	1978-10-16
DE2828604A1 (de)	1979-01-25
AU515469B2 (en)	1981-04-02
CA1088573A (fr)	1980-10-28
IL54925A0 (en)	1978-08-31
IT7809520A0 (it)	1978-07-04

Publication	Publication Date	Title
NO782285L (no)	1979-01-08	Reduksjon av fosfinoksyder.
CA1192908A (fr)	1985-09-03	Preparation d'oximinosilanes, d'oximinogermanes et d'oximinostannanes
US3261871A (en)	1966-07-19	Reduction of phosphine oxides
JPS5921870B2 (ja)	1984-05-22	オルガノ錫化合物の製法
US6160151A (en)	2000-12-12	Process for production of diphenyl-dialkoxysilane, phenylalkyl-dialkoxysilane, octaphenylcyclotetrasilozane and sym-tetraalkyltetraphenyl-cyclotetrasiloxane
US3376347A (en)	1968-04-02	Mono-and di-c-halogenated meta-and paracarborane
US3362977A (en)	1968-01-09	Method for making organosilanes
KR820001182B1 (ko)	1982-06-29	3급포스핀 옥사이드류를 환원하여 3급포스핀을 제조하는 방법
AU635985B2 (en)	1993-04-08	Synthesis of perfluoroalkyl bromides
US4185053A (en)	1980-01-22	Process for manufacturing substantially pure dialkyl phosphorochloridothionate
US2874184A (en)	1959-02-17	Preparation of 1-halophosphonic acids
JPS5949233B2 (ja)	1984-12-01	Ｏ，ｏ−ジアルキルチオノ燐酸クロリドの製造法
US5049691A (en)	1991-09-17	Process for transhalogenating a halophosphorous compound with anhydrous hydrogen fluoride
US2975028A (en)	1961-03-14	Phosphorus compounds and process for making
US3044984A (en)	1962-07-17	Phosphorus containing compounds
US3998886A (en)	1976-12-21	Production of halogen-containing tertiary phosphine oxides
US2654784A (en)	1953-10-06	Method for the manufacture of phosphoric acid anhydrides
US3577482A (en)	1971-05-04	Process for the preparation of thionophosphonates
US4489006A (en)	1984-12-18	Iodopentahydroperfluoroalkyl borates
JPH0222079B2 (fr)	1990-05-17
US4965380A (en)	1990-10-23	Process for preparation of asymmetric triorganotin halide
US3459837A (en)	1969-08-05	Process for preparing aliphatic tertiary phosphites
AU600928B2 (en)	1990-08-30	Preparation of O-alkyl S, S-dialkylphosphorodithioates
US3932524A (en)	1976-01-13	Process for the preparation of phosphine oxides and sulphides
US5136075A (en)	1992-08-04	Process for transhalogenating a halophosphorus compound with fluoride