GB1028173A - Process for the production of organic phosphorus halide complexes - Google Patents
Process for the production of organic phosphorus halide complexesInfo
- Publication number
- GB1028173A GB1028173A GB39650/63A GB3965063A GB1028173A GB 1028173 A GB1028173 A GB 1028173A GB 39650/63 A GB39650/63 A GB 39650/63A GB 3965063 A GB3965063 A GB 3965063A GB 1028173 A GB1028173 A GB 1028173A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phosphorus
- alkyl
- cycloalkyl
- aluminium chloride
- aluminium
- 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.)
- Expired
Links
- -1 phosphorus halide Chemical class 0.000 title abstract 20
- 239000011574 phosphorus Substances 0.000 title abstract 5
- 229910052698 phosphorus Inorganic materials 0.000 title abstract 5
- 229910052783 alkali metal Inorganic materials 0.000 abstract 5
- 150000001340 alkali metals Chemical class 0.000 abstract 5
- 239000000203 mixture Substances 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 239000004411 aluminium Substances 0.000 abstract 3
- 229910052782 aluminium Inorganic materials 0.000 abstract 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- 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 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Chemical group 0.000 abstract 2
- 150000001649 bromium compounds Chemical class 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- 239000011734 sodium Substances 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 1
- PHSPJQZRQAJPPF-UHFFFAOYSA-N N-alpha-Methylhistamine Chemical compound CNCCC1=CN=CN1 PHSPJQZRQAJPPF-UHFFFAOYSA-N 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- QRIYVLHODOYAPU-UHFFFAOYSA-K [Cl-].[Al+3].C(C)P(Br)(Br)(Br)Br.[Cl-].[Cl-] Chemical compound [Cl-].[Al+3].C(C)P(Br)(Br)(Br)Br.[Cl-].[Cl-] QRIYVLHODOYAPU-UHFFFAOYSA-K 0.000 abstract 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 abstract 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 abstract 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 abstract 1
- 150000001347 alkyl bromides Chemical class 0.000 abstract 1
- 150000001348 alkyl chlorides Chemical class 0.000 abstract 1
- 150000001350 alkyl halides Chemical class 0.000 abstract 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium chloride Substances Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 1
- KAGNIVYXCPMHQX-UHFFFAOYSA-K aluminum tetrachloro(trichloromethyl)-lambda5-phosphane trichloride Chemical compound [Cl-].[Al+3].ClC(Cl)(Cl)P(Cl)(Cl)(Cl)Cl.[Cl-].[Cl-] KAGNIVYXCPMHQX-UHFFFAOYSA-K 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- MJEQIIGWDHUZJW-UHFFFAOYSA-N dichloro(cyclohexyl)phosphane Chemical class ClP(Cl)C1CCCCC1 MJEQIIGWDHUZJW-UHFFFAOYSA-N 0.000 abstract 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 229910001537 lithium tetrachloroaluminate Inorganic materials 0.000 abstract 1
- 239000000155 melt Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- UNFUYWDGSFDHCW-UHFFFAOYSA-N monochlorocyclohexane Chemical group ClC1CCCCC1 UNFUYWDGSFDHCW-UHFFFAOYSA-N 0.000 abstract 1
- MPDOUGUGIVBSGZ-UHFFFAOYSA-N n-(cyclobutylmethyl)-3-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC=CC(NCC2CCC2)=C1 MPDOUGUGIVBSGZ-UHFFFAOYSA-N 0.000 abstract 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 229910001538 sodium tetrachloroaluminate Inorganic materials 0.000 abstract 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
-
- 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
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF38030A DE1165596B (de) | 1962-10-13 | 1962-10-13 | Verfahren zur Herstellung von Chlorphosphin-Aluminiumchlorid-Komplexverbindungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1028173A true GB1028173A (en) | 1966-05-04 |
Family
ID=7097184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB39650/63A Expired GB1028173A (en) | 1962-10-13 | 1963-10-08 | Process for the production of organic phosphorus halide complexes |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3329697A (enExample) |
| BE (1) | BE638532A (enExample) |
| DE (1) | DE1165596B (enExample) |
| GB (1) | GB1028173A (enExample) |
| NL (1) | NL299146A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2281288C1 (ru) * | 2005-07-12 | 2006-08-10 | Федеральное государственное образовательное учреждение высшего профессионального образования Чувашский государственный университет им. И.Н. Ульянова | Способ получения комплексов 2-изопропокси-2 метилвинилтрихлорфосфонийгексахлорметаллов |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2986579A (en) * | 1954-03-26 | 1961-05-30 | Universal Oil Prod Co | Preparation of alkylphosphorus dichloride |
-
0
- NL NL299146D patent/NL299146A/xx unknown
- BE BE638532D patent/BE638532A/xx unknown
-
1962
- 1962-10-13 DE DEF38030A patent/DE1165596B/de active Pending
-
1963
- 1963-09-23 US US310912A patent/US3329697A/en not_active Expired - Lifetime
- 1963-10-08 GB GB39650/63A patent/GB1028173A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2281288C1 (ru) * | 2005-07-12 | 2006-08-10 | Федеральное государственное образовательное учреждение высшего профессионального образования Чувашский государственный университет им. И.Н. Ульянова | Способ получения комплексов 2-изопропокси-2 метилвинилтрихлорфосфонийгексахлорметаллов |
Also Published As
| Publication number | Publication date |
|---|---|
| BE638532A (enExample) | |
| DE1165596B (de) | 1964-03-19 |
| NL299146A (enExample) | |
| US3329697A (en) | 1967-07-04 |
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