SU1452476A3 - Способ получени 1,1,2,3-тетрахлорпропена - Google Patents
Способ получени 1,1,2,3-тетрахлорпропена Download PDFInfo
- Publication number
- SU1452476A3 SU1452476A3 SU843757914A SU3757914A SU1452476A3 SU 1452476 A3 SU1452476 A3 SU 1452476A3 SU 843757914 A SU843757914 A SU 843757914A SU 3757914 A SU3757914 A SU 3757914A SU 1452476 A3 SU1452476 A3 SU 1452476A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- tetrachloropropene
- mixture
- ferric chloride
- disclosed
- ppm
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 11
- UMGQVBVEWTXECF-UHFFFAOYSA-N 1,1,2,3-tetrachloroprop-1-ene Chemical compound ClCC(Cl)=C(Cl)Cl UMGQVBVEWTXECF-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000003054 catalyst Substances 0.000 claims abstract description 8
- PQUUGVDRLWLNGR-UHFFFAOYSA-N 2,3,3,3-tetrachloroprop-1-ene Chemical compound ClC(=C)C(Cl)(Cl)Cl PQUUGVDRLWLNGR-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 10
- 238000006317 isomerization reaction Methods 0.000 claims description 5
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 4
- 230000008707 rearrangement Effects 0.000 claims description 4
- GVVUPGXFVJLPDE-OWOJBTEDSA-N (e)-1,3,3,3-tetrachloroprop-1-ene Chemical compound Cl\C=C\C(Cl)(Cl)Cl GVVUPGXFVJLPDE-OWOJBTEDSA-N 0.000 claims description 3
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 claims description 3
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract description 6
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract description 5
- 238000006243 chemical reaction Methods 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 abstract description 3
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- ZXPCCXXSNUIVNK-UHFFFAOYSA-N 1,1,1,2,3-pentachloropropane Chemical compound ClCC(Cl)C(Cl)(Cl)Cl ZXPCCXXSNUIVNK-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 238000007075 allylic rearrangement reaction Methods 0.000 abstract 1
- 238000007033 dehydrochlorination reaction Methods 0.000 abstract 1
- 239000002243 precursor Substances 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OWXJKYNZGFSVRC-NSCUHMNNSA-N (e)-1-chloroprop-1-ene Chemical compound C\C=C\Cl OWXJKYNZGFSVRC-NSCUHMNNSA-N 0.000 description 1
- FTCVHAQNWWBTIV-UHFFFAOYSA-N 1,1,1,2,2-pentachloropropane Chemical compound CC(Cl)(Cl)C(Cl)(Cl)Cl FTCVHAQNWWBTIV-UHFFFAOYSA-N 0.000 description 1
- BUQMVYQMVLAYRU-UHFFFAOYSA-N 1,1,2,3-tetrachloropropane Chemical compound ClCC(Cl)C(Cl)Cl BUQMVYQMVLAYRU-UHFFFAOYSA-N 0.000 description 1
- JRIUOOQEOFUGNA-UHFFFAOYSA-N 1,2,3,3,3-pentachloroprop-1-ene Chemical compound ClC=C(Cl)C(Cl)(Cl)Cl JRIUOOQEOFUGNA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
- 239000005625 Tri-allate Substances 0.000 description 1
- MWBPRDONLNQCFV-UHFFFAOYSA-N Tri-allate Chemical compound CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl MWBPRDONLNQCFV-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 235000014413 iron hydroxide Nutrition 0.000 description 1
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 0.000 description 1
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/272—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions
- C07C17/275—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by addition reactions of hydrocarbons and halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/04—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
- C07C17/358—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by isomerisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
- C07C17/383—Separation; Purification; Stabilisation; Use of additives by distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
- C07C17/383—Separation; Purification; Stabilisation; Use of additives by distillation
- C07C17/386—Separation; Purification; Stabilisation; Use of additives by distillation with auxiliary compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
- C07C21/04—Chloro-alkenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/511,131 US4535194A (en) | 1983-07-06 | 1983-07-06 | Process for producing 1,1,2,3-tetrachloropropene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1452476A3 true SU1452476A3 (ru) | 1989-01-15 |
Family
ID=24033582
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU843757914A SU1452476A3 (ru) | 1983-07-06 | 1984-07-05 | Способ получени 1,1,2,3-тетрахлорпропена |
| SU864000868A SU1470174A3 (ru) | 1983-07-06 | 1986-01-06 | Способ получени 1,1,2,3-тетрахлорпропена |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU864000868A SU1470174A3 (ru) | 1983-07-06 | 1986-01-06 | Способ получени 1,1,2,3-тетрахлорпропена |
Country Status (13)
Families Citing this family (87)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| DE3511153A1 (de) * | 1985-03-27 | 1986-10-02 | Wacker-Chemie GmbH, 8000 München | Verfahren zur herstellung von verbindungen mit mehrfach durch chlor substituiertem alkylrest |
| WO1996016003A1 (fr) * | 1994-11-24 | 1996-05-30 | Solvay (Societe Anonyme) | Procede de conversion d'un alcane chlore en un alcene moins chlore |
| RU2149155C1 (ru) * | 1998-09-04 | 2000-05-20 | Стерлитамакское закрытое акционерное общество "Каустик" | Способ получения непредельных хлоруглеводородов |
| US6534688B2 (en) | 2001-06-11 | 2003-03-18 | Vulcan Chemicals | Dehydrochlorination stabilization of polychlorinated alkanes |
| US6500995B1 (en) | 2001-06-14 | 2002-12-31 | Vulcan Chemicals | Water-enhanced production of 1,1,1,3,3,-pentachloropropane |
| US20050177012A1 (en) * | 2001-07-20 | 2005-08-11 | Pcbu Services, Inc. | Halocarbon production processes, halocarbon separation processes, and halocarbon separation systems |
| US20030028057A1 (en) * | 2001-07-20 | 2003-02-06 | Stephen Owens | Methods and materials for the preparation and purification of halogenated hydrocarbons |
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| PT2231565E (pt) | 2007-12-19 | 2014-06-11 | Occidental Chem Co | Métodos de fabrico de hidrocarbonetos clorados |
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| EP4530279A1 (en) * | 2016-07-26 | 2025-04-02 | Occidental Chemical Corporation | Method for producing halogenated propanes |
| CN112409127A (zh) * | 2020-11-04 | 2021-02-26 | 宁波巨化化工科技有限公司 | 一种四氯乙烯生产过程中的除水方法 |
| CN116265097B (zh) * | 2021-12-17 | 2024-10-08 | 中国科学院宁波材料技术与工程研究所 | 用于气固相反应连续生产1,1,1,3-四氯丙烷的催化剂、其制备方法与应用 |
| CN114105728B (zh) * | 2022-01-25 | 2022-04-12 | 北京宇极科技发展有限公司 | 同时制备e-1,3,3,3-四氯丙烯和1,1,3,3-四氯丙烯的方法 |
| CN115722255B (zh) * | 2022-10-13 | 2024-08-27 | 浙江衢化氟化学有限公司 | 一种用于生产1,1,1,2,3-五氯丙烷的负载型催化剂及其制备方法和应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE36503C (de) * | E. PERGANDE in Perleberg | Windregulirvorrichtung für Schmiedefeuer und dergl | ||
| US2420975A (en) * | 1943-05-27 | 1947-05-20 | Pennsylvania Salt Mfg Co | Process of producing a solid pentachloropropane |
| US2593451A (en) * | 1947-06-25 | 1952-04-22 | Dow Chemical Co | Dehydrochlorination of polychloroethanes |
| US2561516A (en) * | 1948-02-20 | 1951-07-24 | Us Rubber Co | Trichloromethylalkenes |
| US2658930A (en) * | 1949-03-22 | 1953-11-10 | Universal Oil Prod Co | Production of polyhaloalkanes |
| DE1027648B (de) * | 1954-02-03 | 1958-04-10 | Hoechst Ag | Verfahren zur Herstellung von halogenierten Alkanen |
| US3639493A (en) * | 1968-02-28 | 1972-02-01 | Du Pont | Dehydrohalogenation of halogenated compounds |
| US3926758A (en) * | 1971-12-27 | 1975-12-16 | Monsanto Co | Preparation of 1,1,2,3-tetrachloropropene from 2,3-trichloropropane |
| JPS4966613A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-10-27 | 1974-06-27 | ||
| JPS516641A (en) * | 1974-07-04 | 1976-01-20 | Tektronix Inc | Zofukutokuseino kahenna zofukuki |
| JPS5929042B2 (ja) * | 1975-07-09 | 1984-07-18 | 株式会社トクヤマ | パ−ハロゲン化アルカンとオレフイン類との付加反応方法 |
| JPS5259103A (en) * | 1975-11-10 | 1977-05-16 | Shin Etsu Chem Co Ltd | Process for preparation of tetrachloroalkane |
| SU899523A1 (ru) * | 1979-07-03 | 1982-01-23 | Уфимский Нефтяной Институт | Способ получени 1,1,2,3-тетрахлорпропена |
| DE3007634C2 (de) * | 1980-02-29 | 1982-08-19 | Hans-Jürgen Dipl.-Chem. Dr. 7808 Waldkirch Pettelkau | Verfahren zur Herstellung von Vinylchlorid |
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1983
- 1983-07-06 US US06/511,131 patent/US4535194A/en not_active Expired - Lifetime
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1984
- 1984-07-04 DE DE8484870092T patent/DE3465290D1/de not_active Expired
- 1984-07-04 EP EP84870092A patent/EP0131560B1/en not_active Expired
- 1984-07-04 AT AT84870092T patent/ATE28853T1/de not_active IP Right Cessation
- 1984-07-05 SU SU843757914A patent/SU1452476A3/ru active
- 1984-07-05 KR KR1019840003899A patent/KR850001144A/ko not_active Abandoned
- 1984-07-05 HU HU842648A patent/HUT34422A/hu unknown
- 1984-07-05 AU AU30318/84A patent/AU3031884A/en not_active Abandoned
- 1984-07-05 ZA ZA845179A patent/ZA845179B/xx unknown
- 1984-07-05 DK DK329784A patent/DK329784A/da not_active Application Discontinuation
- 1984-07-05 IL IL72305A patent/IL72305A0/xx unknown
- 1984-07-05 JP JP59138112A patent/JPS6036429A/ja active Granted
- 1984-07-05 CA CA000458213A patent/CA1230132A/en not_active Expired
-
1986
- 1986-01-06 SU SU864000868A patent/SU1470174A3/ru active
Non-Patent Citations (1)
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| Haszeldine, Tluoroolefins, Journ Chem, Soc., 1953, c.3371-3378, Авторское свидетельство СССР № 899523, кл.С 07 С 21/04, 1979. * |
Also Published As
| Publication number | Publication date |
|---|---|
| KR850001144A (ko) | 1985-03-16 |
| SU1470174A3 (ru) | 1989-03-30 |
| ATE28853T1 (de) | 1987-08-15 |
| EP0131560A1 (en) | 1985-01-16 |
| DK329784A (da) | 1985-01-07 |
| HUT34422A (en) | 1985-03-28 |
| EP0131560B1 (en) | 1987-08-12 |
| DE3465290D1 (en) | 1987-09-17 |
| JPS6036429A (ja) | 1985-02-25 |
| CA1230132A (en) | 1987-12-08 |
| IL72305A0 (en) | 1984-11-30 |
| DK329784D0 (da) | 1984-07-05 |
| AU3031884A (en) | 1985-01-10 |
| US4535194A (en) | 1985-08-13 |
| ZA845179B (en) | 1985-03-27 |
| JPH0247969B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-10-23 |
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