FR1304533A - Procédé de préparation de composés organiques phosphorés - Google Patents
Procédé de préparation de composés organiques phosphorésInfo
- Publication number
- FR1304533A FR1304533A FR877123A FR877123A FR1304533A FR 1304533 A FR1304533 A FR 1304533A FR 877123 A FR877123 A FR 877123A FR 877123 A FR877123 A FR 877123A FR 1304533 A FR1304533 A FR 1304533A
- Authority
- FR
- France
- Prior art keywords
- phosphine
- butylbis
- trifluoromethylphenyl
- dibutyl
- naphthyl
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- 150000002903 organophosphorus compounds Chemical class 0.000 title 1
- 150000001350 alkyl halides Chemical class 0.000 abstract 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 2
- DGTLHEXJPUJELR-UHFFFAOYSA-N butyl-bis[3-(trifluoromethyl)phenyl]phosphane Chemical compound C(CCC)P(C1=CC(=CC=C1)C(F)(F)F)C1=CC(=CC=C1)C(F)(F)F DGTLHEXJPUJELR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000003003 phosphines Chemical class 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- VXLQXFQDOGUAPA-UHFFFAOYSA-N (4-methoxyphenyl)phosphane Chemical compound COC1=CC=C(P)C=C1 VXLQXFQDOGUAPA-UHFFFAOYSA-N 0.000 abstract 1
- IWPZVUTXBXPWSN-UHFFFAOYSA-N (6-methoxynaphthalen-2-yl)-dimethylphosphane Chemical compound CP(C1=CC2=CC=C(C=C2C=C1)OC)C IWPZVUTXBXPWSN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 abstract 1
- DLKQHBOKULLWDQ-UHFFFAOYSA-N 1-bromonaphthalene Chemical compound C1=CC=C2C(Br)=CC=CC2=C1 DLKQHBOKULLWDQ-UHFFFAOYSA-N 0.000 abstract 1
- URGSMJLDEFDWNX-UHFFFAOYSA-N 1-butylnaphthalene Chemical compound C1=CC=C2C(CCCC)=CC=CC2=C1 URGSMJLDEFDWNX-UHFFFAOYSA-N 0.000 abstract 1
- YEVQLUVJMKDGKL-UHFFFAOYSA-N C(CCC)P(C1=CC=C(C=C1)F)C1=CC=C(C=C1)F Chemical compound C(CCC)P(C1=CC=C(C=C1)F)C1=CC=C(C=C1)F YEVQLUVJMKDGKL-UHFFFAOYSA-N 0.000 abstract 1
- ZATOFRITFRPYBT-UHFFFAOYSA-N C1=CC=C2C([Li])=CC=CC2=C1 Chemical compound C1=CC=C2C([Li])=CC=CC2=C1 ZATOFRITFRPYBT-UHFFFAOYSA-N 0.000 abstract 1
- 229910010084 LiAlH4 Inorganic materials 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- PBDHWRDKOOAAGK-UHFFFAOYSA-N bis(6-methoxynaphthalen-2-yl)-methylphosphane Chemical compound COC=1C=C2C=CC(=CC2=CC1)P(C)C1=CC2=CC=C(C=C2C=C1)OC PBDHWRDKOOAAGK-UHFFFAOYSA-N 0.000 abstract 1
- BMXYPKZGVBZXPT-UHFFFAOYSA-N butyl(dinaphthalen-1-yl)phosphane Chemical compound C1=CC=C2C(P(C=3C4=CC=CC=C4C=CC=3)CCCC)=CC=CC2=C1 BMXYPKZGVBZXPT-UHFFFAOYSA-N 0.000 abstract 1
- WXMZPPIDLJRXNK-UHFFFAOYSA-N butyl(diphenyl)phosphane Chemical compound C=1C=CC=CC=1P(CCCC)C1=CC=CC=C1 WXMZPPIDLJRXNK-UHFFFAOYSA-N 0.000 abstract 1
- LMTGBYGAFQTBDR-UHFFFAOYSA-N butyl(naphthalen-1-yl)phosphane Chemical compound C1=CC=C2C(PCCCC)=CC=CC2=C1 LMTGBYGAFQTBDR-UHFFFAOYSA-N 0.000 abstract 1
- PVWYTIFUYYJMQO-UHFFFAOYSA-N butyl(phenyl)phosphane Chemical compound CCCCPC1=CC=CC=C1 PVWYTIFUYYJMQO-UHFFFAOYSA-N 0.000 abstract 1
- ZUJWQEHMSSAYFV-UHFFFAOYSA-N butyl-(4-fluorophenyl)phosphane Chemical compound C(CCC)PC1=CC=C(C=C1)F ZUJWQEHMSSAYFV-UHFFFAOYSA-N 0.000 abstract 1
- XEGQLOAOJPOXIA-UHFFFAOYSA-N butyl-bis(4-methoxyphenyl)phosphane Chemical compound C=1C=C(OC)C=CC=1P(CCCC)C1=CC=C(OC)C=C1 XEGQLOAOJPOXIA-UHFFFAOYSA-N 0.000 abstract 1
- DLIJPAHLBJIQHE-UHFFFAOYSA-N butylphosphane Chemical compound CCCCP DLIJPAHLBJIQHE-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- OTFXOBKITKKHRS-UHFFFAOYSA-N cyclohexyl(dihexyl)phosphane Chemical compound CCCCCCP(CCCCCC)C1CCCCC1 OTFXOBKITKKHRS-UHFFFAOYSA-N 0.000 abstract 1
- ZBCKWHYWPLHBOK-UHFFFAOYSA-N cyclohexylphosphane Chemical compound PC1CCCCC1 ZBCKWHYWPLHBOK-UHFFFAOYSA-N 0.000 abstract 1
- ORICWOYODJGJMY-UHFFFAOYSA-N dibutyl(phenyl)phosphane Chemical compound CCCCP(CCCC)C1=CC=CC=C1 ORICWOYODJGJMY-UHFFFAOYSA-N 0.000 abstract 1
- IWAUQEUOKFBSTQ-UHFFFAOYSA-N dibutyl-(4-fluorophenyl)phosphane Chemical compound C(CCC)P(C1=CC=C(C=C1)F)CCCC IWAUQEUOKFBSTQ-UHFFFAOYSA-N 0.000 abstract 1
- OWLQYARBQTXCDD-UHFFFAOYSA-N dibutyl-(4-methoxyphenyl)phosphane Chemical compound CCCCP(CCCC)C1=CC=C(OC)C=C1 OWLQYARBQTXCDD-UHFFFAOYSA-N 0.000 abstract 1
- NCXVVTDUSUAOHO-UHFFFAOYSA-N dibutyl-[3-(trifluoromethyl)phenyl]phosphane Chemical compound C(CCC)P(C1=CC(=CC=C1)C(F)(F)F)CCCC NCXVVTDUSUAOHO-UHFFFAOYSA-N 0.000 abstract 1
- PTLIZOFGXLGHSY-UHFFFAOYSA-N dibutylphosphane Chemical compound CCCCPCCCC PTLIZOFGXLGHSY-UHFFFAOYSA-N 0.000 abstract 1
- MESBJEBWWDYMSJ-UHFFFAOYSA-N dicyclohexyl(hexyl)phosphane Chemical compound C1CCCCC1P(CCCCCC)C1CCCCC1 MESBJEBWWDYMSJ-UHFFFAOYSA-N 0.000 abstract 1
- -1 dinaphthylphosphine Chemical compound 0.000 abstract 1
- BYYQOWAAZOHHFN-UHFFFAOYSA-N dioctylphosphane Chemical compound CCCCCCCCPCCCCCCCC BYYQOWAAZOHHFN-UHFFFAOYSA-N 0.000 abstract 1
- GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 abstract 1
- AAKDVDDBABPPKC-UHFFFAOYSA-N dodecylphosphane Chemical compound CCCCCCCCCCCCP AAKDVDDBABPPKC-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- AAWKVSBCMBPJPP-UHFFFAOYSA-N hexyl(dimethyl)phosphane Chemical compound CCCCCCP(C)C AAWKVSBCMBPJPP-UHFFFAOYSA-N 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- FVWCDFMLOYFXCE-UHFFFAOYSA-N naphthalen-1-ylphosphane Chemical compound C1=CC=C2C(P)=CC=CC2=C1 FVWCDFMLOYFXCE-UHFFFAOYSA-N 0.000 abstract 1
- SWMBQMGPRYJSCI-UHFFFAOYSA-N octylphosphane Chemical compound CCCCCCCCP SWMBQMGPRYJSCI-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 150000002902 organometallic compounds Chemical class 0.000 abstract 1
- NEBORWPMFGNHSJ-UHFFFAOYSA-N pentyl(dipropyl)phosphane Chemical compound CCCCCP(CCC)CCC NEBORWPMFGNHSJ-UHFFFAOYSA-N 0.000 abstract 1
- RPGWZZNNEUHDAQ-UHFFFAOYSA-N phenylphosphine Chemical compound PC1=CC=CC=C1 RPGWZZNNEUHDAQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 abstract 1
- GRAKJTASWCEOQI-UHFFFAOYSA-N tridodecylphosphane Chemical compound CCCCCCCCCCCCP(CCCCCCCCCCCC)CCCCCCCCCCCC GRAKJTASWCEOQI-UHFFFAOYSA-N 0.000 abstract 1
- FPZZZGJWXOHLDJ-UHFFFAOYSA-N trihexylphosphane Chemical compound CCCCCCP(CCCCCC)CCCCCC FPZZZGJWXOHLDJ-UHFFFAOYSA-N 0.000 abstract 1
- DMEUUKUNSVFYAA-UHFFFAOYSA-N trinaphthalen-1-ylphosphane Chemical compound C1=CC=C2C(P(C=3C4=CC=CC=C4C=CC=3)C=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 DMEUUKUNSVFYAA-UHFFFAOYSA-N 0.000 abstract 1
- RMZAYIKUYWXQPB-UHFFFAOYSA-N trioctylphosphane Chemical compound CCCCCCCCP(CCCCCCCC)CCCCCCCC RMZAYIKUYWXQPB-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/26—Organic compounds containing phosphorus
- C10L1/2608—Organic compounds containing phosphorus containing a phosphorus-carbon bond
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6788460A | 1960-11-08 | 1960-11-08 | |
| US67883A US3060241A (en) | 1960-11-08 | 1960-11-08 | Preparation of alkyl cycloalkyl and aromatic phosphines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| FR1304533A true FR1304533A (fr) | 1962-09-21 |
Family
ID=26748370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR877123A Expired FR1304533A (fr) | 1960-11-08 | 1961-10-26 | Procédé de préparation de composés organiques phosphorés |
Country Status (3)
| Country | Link |
|---|---|
| DE (2) | DE1197449B (fr) |
| FR (1) | FR1304533A (fr) |
| GB (1) | GB944062A (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110494497B (zh) | 2017-08-04 | 2021-11-09 | 瓦克化学股份公司 | 可以通过uv光辐照交联的硅酮组合物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2900416A (en) * | 1956-02-21 | 1959-08-18 | American Potash & Chem Corp | Method of preparation of alkyl-substituted phosphines |
| SU130512A1 (ru) * | 1960-02-15 | 1960-11-30 | В.И. Емельянов | Способ получени алкил и (арил) дигалоидфосфинов и диалкил и (диарил) галоидофосфинов |
-
1961
- 1961-10-19 GB GB3749561A patent/GB944062A/en not_active Expired
- 1961-10-26 FR FR877123A patent/FR1304533A/fr not_active Expired
- 1961-11-08 DE DEA38780A patent/DE1197449B/de active Pending
- 1961-11-08 DE DEA47748A patent/DE1201836B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| GB944062A (en) | 1963-12-11 |
| DE1201836B (de) | 1965-09-30 |
| DE1197449B (de) | 1965-07-29 |
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