DE1165597B - Verfahren zur Herstellung von organischen Phosphinhalogeniden - Google Patents
Verfahren zur Herstellung von organischen PhosphinhalogenidenInfo
- Publication number
- DE1165597B DE1165597B DEF38062A DEF0038062A DE1165597B DE 1165597 B DE1165597 B DE 1165597B DE F38062 A DEF38062 A DE F38062A DE F0038062 A DEF0038062 A DE F0038062A DE 1165597 B DE1165597 B DE 1165597B
- Authority
- DE
- Germany
- Prior art keywords
- halide
- melt
- organic phosphine
- chloride
- complex
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- -1 phosphine halides Chemical class 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 15
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 title claims description 7
- 229910000073 phosphorus hydride Inorganic materials 0.000 title claims description 7
- 238000002360 preparation method Methods 0.000 title description 4
- 239000000460 chlorine Substances 0.000 claims description 17
- 229910052801 chlorine Inorganic materials 0.000 claims description 13
- 239000000155 melt Substances 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 7
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 6
- 239000011574 phosphorus Substances 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000011780 sodium chloride Substances 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000001103 potassium chloride Substances 0.000 claims description 3
- 235000011164 potassium chloride Nutrition 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 238000004821 distillation Methods 0.000 claims description 2
- 150000002484 inorganic compounds Chemical class 0.000 claims description 2
- 229910010272 inorganic material Inorganic materials 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 22
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 13
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 238000005868 electrolysis reaction Methods 0.000 description 8
- 229910001538 sodium tetrachloroaluminate Inorganic materials 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 229910052759 nickel Inorganic materials 0.000 description 6
- 229910052721 tungsten Inorganic materials 0.000 description 6
- 239000010937 tungsten Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 5
- 239000004927 clay Substances 0.000 description 4
- JHNJGLVSPIMBLD-UHFFFAOYSA-N dichloro(ethyl)phosphane Chemical compound CCP(Cl)Cl JHNJGLVSPIMBLD-UHFFFAOYSA-N 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229910016467 AlCl 4 Inorganic materials 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RFJHCAHSOWEFNE-UHFFFAOYSA-N benzyl(chloro)phosphane Chemical compound ClPCC1=CC=CC=C1 RFJHCAHSOWEFNE-UHFFFAOYSA-N 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- BPQGJGHGCWPAFA-UHFFFAOYSA-N dibromo(methyl)phosphane Chemical compound CP(Br)Br BPQGJGHGCWPAFA-UHFFFAOYSA-N 0.000 description 2
- IMDXZWRLUZPMDH-UHFFFAOYSA-N dichlorophenylphosphine Chemical compound ClP(Cl)C1=CC=CC=C1 IMDXZWRLUZPMDH-UHFFFAOYSA-N 0.000 description 2
- LWNLXVXSCCLRRZ-UHFFFAOYSA-N dichlorophosphane Chemical compound ClPCl LWNLXVXSCCLRRZ-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000011152 fibreglass Substances 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- 239000007788 liquid Chemical class 0.000 description 2
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- PUGUQINMNYINPK-UHFFFAOYSA-N tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCN(C(=O)CCl)CC1 PUGUQINMNYINPK-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 description 1
- 101100462611 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) prr-1 gene Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- DCZYNCBXNNXSNR-UHFFFAOYSA-K [Cl-].[Al+3].C(C)P(Cl)(Cl)(Cl)CC.[Cl-].[Cl-] Chemical compound [Cl-].[Al+3].C(C)P(Cl)(Cl)(Cl)CC.[Cl-].[Cl-] DCZYNCBXNNXSNR-UHFFFAOYSA-K 0.000 description 1
- DJJOUILAPXFQMO-UHFFFAOYSA-K [Cl-].[Al+3].C(C)P(Cl)(Cl)(Cl)Cl.[Cl-].[Cl-] Chemical compound [Cl-].[Al+3].C(C)P(Cl)(Cl)(Cl)Cl.[Cl-].[Cl-] DJJOUILAPXFQMO-UHFFFAOYSA-K 0.000 description 1
- IUPSYSRBOJKLLY-UHFFFAOYSA-K [Cl-].[Al+3].C1(CCCCC1)P(Cl)(Cl)(Cl)Cl.[Cl-].[Cl-] Chemical compound [Cl-].[Al+3].C1(CCCCC1)P(Cl)(Cl)(Cl)Cl.[Cl-].[Cl-] IUPSYSRBOJKLLY-UHFFFAOYSA-K 0.000 description 1
- CPNWPWZLPUVOCF-UHFFFAOYSA-O [ClH]1[AlH]C(=CC=C1)C(=O)O Chemical compound [ClH]1[AlH]C(=CC=C1)C(=O)O CPNWPWZLPUVOCF-UHFFFAOYSA-O 0.000 description 1
- IZPZQHISQHRLFP-UHFFFAOYSA-J [Na+].[Na+].[Na+].[Na+].[Cl-].[Cl-].[Cl-].[Cl-] Chemical compound [Na+].[Na+].[Na+].[Na+].[Cl-].[Cl-].[Cl-].[Cl-] IZPZQHISQHRLFP-UHFFFAOYSA-J 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- BYOALROSGCAZLO-UHFFFAOYSA-K aluminum chlorophosphane trichloride Chemical compound [Cl-].[Al+3].ClP.[Cl-].[Cl-] BYOALROSGCAZLO-UHFFFAOYSA-K 0.000 description 1
- 239000010405 anode material Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- MJEQIIGWDHUZJW-UHFFFAOYSA-N dichloro(cyclohexyl)phosphane Chemical compound ClP(Cl)C1CCCCC1 MJEQIIGWDHUZJW-UHFFFAOYSA-N 0.000 description 1
- CDPKWOKGVUHZFR-UHFFFAOYSA-N dichloro(methyl)phosphane Chemical compound CP(Cl)Cl CDPKWOKGVUHZFR-UHFFFAOYSA-N 0.000 description 1
- VRSASSVPDGYCTJ-UHFFFAOYSA-N dichloro(phenyl)phosphane hydrochloride Chemical compound C1=CC=C(C=C1)P(Cl)Cl.Cl VRSASSVPDGYCTJ-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- UNFUYWDGSFDHCW-UHFFFAOYSA-N monochlorocyclohexane Chemical compound ClC1CCCCC1 UNFUYWDGSFDHCW-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint 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
- 238000010992 reflux Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000003466 welding 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
- C07F9/52—Halophosphines
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/25—Reduction
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrolytic Production Of Metals (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL299393D NL299393A (ref) | 1962-10-17 | ||
| BE638709D BE638709A (ref) | 1962-10-17 | ||
| DEF38062A DE1165597B (de) | 1962-10-17 | 1962-10-17 | Verfahren zur Herstellung von organischen Phosphinhalogeniden |
| US309386A US3312606A (en) | 1962-10-17 | 1963-09-17 | Process for the production of organic phosphine halides |
| GB38236/63A GB1031839A (en) | 1962-10-17 | 1963-09-27 | Process for the electrolytic production of organic phosphine halides |
| FR950718A FR1373933A (fr) | 1962-10-17 | 1963-10-16 | Procédé de préparation d'halogénophosphines organiques |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF38062A DE1165597B (de) | 1962-10-17 | 1962-10-17 | Verfahren zur Herstellung von organischen Phosphinhalogeniden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1165597B true DE1165597B (de) | 1964-03-19 |
Family
ID=7097196
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF38062A Pending DE1165597B (de) | 1962-10-17 | 1962-10-17 | Verfahren zur Herstellung von organischen Phosphinhalogeniden |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3312606A (ref) |
| BE (1) | BE638709A (ref) |
| DE (1) | DE1165597B (ref) |
| GB (1) | GB1031839A (ref) |
| NL (1) | NL299393A (ref) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0105053D0 (en) * | 2001-03-01 | 2001-04-18 | Rhodia Cons Spec Ltd | Halogenated phosphines |
| US7053232B2 (en) * | 2002-08-16 | 2006-05-30 | Sachem, Inc. | Lewis acid ionic liquids |
| CN112499587A (zh) * | 2020-11-30 | 2021-03-16 | 洪湖市一泰科技有限公司 | 一种甲基二氯膦及甲基亚膦酸二乙酯生产过程中产生的副产物的协同处理方法 |
-
0
- BE BE638709D patent/BE638709A/xx unknown
- NL NL299393D patent/NL299393A/xx unknown
-
1962
- 1962-10-17 DE DEF38062A patent/DE1165597B/de active Pending
-
1963
- 1963-09-17 US US309386A patent/US3312606A/en not_active Expired - Lifetime
- 1963-09-27 GB GB38236/63A patent/GB1031839A/en not_active Expired
Non-Patent Citations (1)
| Title |
|---|
| None * |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1031839A (en) | 1966-06-02 |
| NL299393A (ref) | |
| US3312606A (en) | 1967-04-04 |
| BE638709A (ref) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2861030A (en) | Electrolytic production of multivalent metals from refractory oxides | |
| DE1047450B (de) | Elektrolyt zur elektrolytischen Abscheidung von Aluminium | |
| DE2251262C2 (de) | Verfahren zur kontinuierlichen Aluminiumherstellung durch Elektrolyse von Aluminiumchlorid | |
| DE1259883B (de) | Verfahren zur Herstellung von Trikohlenwasserstoffphosphinen | |
| DE1165597B (de) | Verfahren zur Herstellung von organischen Phosphinhalogeniden | |
| Budnikova et al. | Arylation and alkylation of white phosphorus in the presence of electrochemically generated nickel (0) complexes | |
| EP0684248A1 (de) | Verfahren zur Herstellung von tertiären Diarylalkylphosphinen | |
| US2734855A (en) | Electrolytic preparation of reduced | |
| US4510095A (en) | Production of organotin halides | |
| DE2713236A1 (de) | Verfahren zur herstellung basischer aluminiumchloride | |
| CA1214428A (en) | Electrolysis of tin complexes | |
| DE102004036853A1 (de) | Verfahren zur Herstellung von Alkylboronsäureestern | |
| US3630858A (en) | A.c. electrolytic process | |
| EP1668172A2 (de) | Elektrochemisches verfahren zur herstellung von diphenylphosphinoxid, diphenylphophin oder phosphin und deren derivaten | |
| US4021321A (en) | Electrolytic preparation of phosphorous acid from elemental phosphorus | |
| AT282210B (de) | Verfahren und Vorrichtung zur Herstellung von Aluminium und Aluminiumlegierungen | |
| DE19526464C1 (de) | Chirale tertiäre Phosphine und Verfahren zu ihrer Herstellung | |
| DE19641526A1 (de) | Verfahren zur elektrochemischen Herstellung von Trialkylphosphaten | |
| DE2721038C3 (de) | Verfahren zur elektrolytischen Herstellung von Aluminium | |
| US4021322A (en) | Electrolytic preparation of phosphorus acid from elemental phosphorus | |
| DE1146258B (de) | Metallorganischer Elektrolyt hoher Leitfaehigkeit zur kathodischen Abscheidung von Natrium | |
| EP0308744B1 (de) | Verfahren zur Herstellung von Imidazolidinonen und Oxazolidinonen | |
| DE102011007559A1 (de) | Verfahren zur Herstellung von Elektrolyten für die Aluminiumabscheidung | |
| Tomilov et al. | Electrochemical alkylation of diethylphosphite | |
| JPH0841672A (ja) | ４，４’−ジメチル−１，１’−ビナフチルの製造方法 |