JPS59108727A - 改良脱ハロゲン化水素法 - Google Patents
改良脱ハロゲン化水素法Info
- Publication number
- JPS59108727A JPS59108727A JP58220895A JP22089583A JPS59108727A JP S59108727 A JPS59108727 A JP S59108727A JP 58220895 A JP58220895 A JP 58220895A JP 22089583 A JP22089583 A JP 22089583A JP S59108727 A JPS59108727 A JP S59108727A
- Authority
- JP
- Japan
- Prior art keywords
- reactor
- carbon atoms
- alkali
- hydrocarbon
- fed
- 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.)
- Granted
Links
- 238000005695 dehalogenation reaction Methods 0.000 title 1
- 238000005984 hydrogenation reaction Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims description 33
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 21
- 238000006243 chemical reaction Methods 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000003513 alkali Substances 0.000 claims description 11
- 239000003054 catalyst Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000012074 organic phase Substances 0.000 claims description 9
- 239000000243 solution Substances 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000012267 brine Substances 0.000 claims description 6
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 239000002699 waste material Substances 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 239000007858 starting material Substances 0.000 claims description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- -1 chloride quaternary ammonium salt Chemical class 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 230000005284 excitation Effects 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims 1
- 239000012071 phase Substances 0.000 description 8
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 7
- 150000008282 halocarbons Chemical class 0.000 description 7
- 239000003444 phase transfer catalyst Substances 0.000 description 6
- 239000008346 aqueous phase Substances 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical group [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- XVEASTGLHPVZNA-UHFFFAOYSA-N 3,4-dichlorobut-1-ene Chemical compound ClCC(Cl)C=C XVEASTGLHPVZNA-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 150000002500 ions Chemical group 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 238000003408 phase transfer catalysis Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- WZUZDBPJFHQVJC-UHFFFAOYSA-N 2,3,4-trichlorobut-1-ene Chemical compound ClCC(Cl)C(Cl)=C WZUZDBPJFHQVJC-UHFFFAOYSA-N 0.000 description 1
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- 238000003287 bathing Methods 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
- 238000004364 calculation method Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000034303 cell budding Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- NRNCYVBFPDDJNE-UHFFFAOYSA-N pemoline Chemical compound O1C(N)=NC(=O)C1C1=CC=CC=C1 NRNCYVBFPDDJNE-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US445155 | 1982-11-29 | ||
| US06/445,155 US4418232A (en) | 1982-11-29 | 1982-11-29 | Dehydrohalogenation process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59108727A true JPS59108727A (ja) | 1984-06-23 |
| JPH0146496B2 JPH0146496B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1989-10-09 |
Family
ID=23767816
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58220895A Granted JPS59108727A (ja) | 1982-11-29 | 1983-11-25 | 改良脱ハロゲン化水素法 |
Country Status (6)
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62148441A (ja) * | 1985-12-23 | 1987-07-02 | Mitsui Toatsu Chem Inc | アルケニルフェノ−ルの製造方法 |
| WO1994014736A1 (en) * | 1992-12-29 | 1994-07-07 | Daikin Industries, Ltd. | Process for producing 1,1,1,3,3-pentafluoropropane, process for producing 1,1,1,3,3-pentafluoro-2-halogeno-3-chloropropane, and process for producing 1,1,1,2,3,3-hexachloropropene |
| JP2007169276A (ja) * | 2005-12-22 | 2007-07-05 | Solvay Solexis Spa | フルオロハロゲンエーテルの製造方法 |
| JP2007169275A (ja) * | 2005-12-22 | 2007-07-05 | Solvay Solexis Spa | フルオロハロゲンエーテルの製造方法 |
| JP2010229092A (ja) * | 2009-03-27 | 2010-10-14 | Tokuyama Corp | トリクロロプロペンの製造方法 |
| WO2015166961A1 (ja) * | 2014-04-28 | 2015-11-05 | ダイキン工業株式会社 | １，１，２－トリブロモエタンの製造方法 |
| JP2015221778A (ja) * | 2014-04-28 | 2015-12-10 | ダイキン工業株式会社 | １，１，２−トリブロモエタンの製造方法 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5237114A (en) * | 1992-03-20 | 1993-08-17 | E. I. Du Pont De Nemours And Company | Removal of catalyst from chloroprene by treatment with oxy acid |
| US5396002A (en) * | 1993-08-18 | 1995-03-07 | The Dow Chemical Company | Process to produce vinylidene chloride using phase transfer catalyst |
| US6380446B1 (en) | 2000-08-17 | 2002-04-30 | Dupont Dow Elastomers, L.L.C. | Process for dehydrohalogenation of halogenated compounds |
| US8969645B2 (en) * | 2012-12-14 | 2015-03-03 | Chevron U.S.A. Inc. | Process for reducing chloride in hydrocarbon products using an ionic liquid catalyst |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3981937A (en) * | 1966-06-03 | 1976-09-21 | E. I. Du Pont De Nemours And Company | Dehydrohalogenation of 3,4-dichloro-1-butene |
| US3754044A (en) * | 1968-02-28 | 1973-08-21 | Du Pont | Dehydrohalogenation of halogenated compounds |
-
1982
- 1982-11-29 US US06/445,155 patent/US4418232A/en not_active Expired - Lifetime
-
1983
- 1983-11-24 CA CA000441830A patent/CA1207803A/en not_active Expired
- 1983-11-25 JP JP58220895A patent/JPS59108727A/ja active Granted
- 1983-11-28 SU SU833666211A patent/SU1277888A3/ru active
- 1983-11-29 EP EP83111953A patent/EP0110377B1/en not_active Expired
- 1983-11-29 DE DE8383111953T patent/DE3361129D1/de not_active Expired
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62148441A (ja) * | 1985-12-23 | 1987-07-02 | Mitsui Toatsu Chem Inc | アルケニルフェノ−ルの製造方法 |
| WO1994014736A1 (en) * | 1992-12-29 | 1994-07-07 | Daikin Industries, Ltd. | Process for producing 1,1,1,3,3-pentafluoropropane, process for producing 1,1,1,3,3-pentafluoro-2-halogeno-3-chloropropane, and process for producing 1,1,1,2,3,3-hexachloropropene |
| JP2007169276A (ja) * | 2005-12-22 | 2007-07-05 | Solvay Solexis Spa | フルオロハロゲンエーテルの製造方法 |
| JP2007169275A (ja) * | 2005-12-22 | 2007-07-05 | Solvay Solexis Spa | フルオロハロゲンエーテルの製造方法 |
| JP2010229092A (ja) * | 2009-03-27 | 2010-10-14 | Tokuyama Corp | トリクロロプロペンの製造方法 |
| WO2015166961A1 (ja) * | 2014-04-28 | 2015-11-05 | ダイキン工業株式会社 | １，１，２－トリブロモエタンの製造方法 |
| JP2015221778A (ja) * | 2014-04-28 | 2015-12-10 | ダイキン工業株式会社 | １，１，２−トリブロモエタンの製造方法 |
| CN106458797A (zh) * | 2014-04-28 | 2017-02-22 | 大金工业株式会社 | 1，1，2‑三溴乙烷的制造方法 |
| CN106458797B (zh) * | 2014-04-28 | 2019-05-10 | 大金工业株式会社 | 1，1，2-三溴乙烷的制造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US4418232A (en) | 1983-11-29 |
| JPH0146496B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1989-10-09 |
| CA1207803A (en) | 1986-07-15 |
| EP0110377A1 (en) | 1984-06-13 |
| SU1277888A3 (ru) | 1986-12-15 |
| DE3361129D1 (en) | 1985-12-05 |
| EP0110377B1 (en) | 1985-10-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU748266B2 (en) | Methods for converting lower alkanes and alkenes to alcohols and diols | |
| US5185479A (en) | Process for methyl alcohol | |
| US4661648A (en) | Process for carrying out substitution chlorination reactions of organic compounds by means of molecular chlorine in the presence of a chlorinated product serving as a radical initiator, and radical initiators used in such a process | |
| US7091391B2 (en) | Methane to olefins | |
| KR19980087226A (ko) | 알킬 모노할로겐화물의 가수분해 방법 | |
| JPS59108727A (ja) | 改良脱ハロゲン化水素法 | |
| EP0086822A1 (en) | METHOD FOR THE PRODUCTION OF METHYL HALIDES AND METHYL ALCOHOL FROM METHANE. | |
| US20020022753A1 (en) | Process for dehydrohalogenation of halog enated compounds | |
| JP2019501914A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| EP3770139A1 (en) | Improved processes for preparing halogenated alkanes | |
| US2216548A (en) | Process for production of unsaturated amines | |
| WO2020041667A1 (en) | One pot dehydrochlorination/chlorination of a chloroalkane to produce a mixture of chlorinated alkenes and chlorinated alkanes | |
| JPH06298701A (ja) | 蟻酸メチルの製法 | |
| Luker et al. | The tandem insertion of allyl carbenoids and aldehydes or ketones into zirconacyclopentanes: Variation of the allyl Moiety and functionalisation of the final carbon-zirconium bond | |
| JP2572002B2 (ja) | フルオレノンの製造方法 | |
| US2475364A (en) | Catalytic hydrolysis of unsaturated halides | |
| JPH08245439A (ja) | ハロゲン化炭化水素の接触脱ハロゲン化水素のための方法 | |
| RU2125551C1 (ru) | Способ получения смеси 1-хлор- и 1,3-дихлорадамантанов | |
| KR19990083343A (ko) | 기체상알칸의광화학적설포클로로화방법 | |
| EP0052727B1 (en) | Process for brominating side chain of m-phenoxytoluene | |
| CN119118783A (zh) | 用于由d-d混剂制备1,1,2,3-四氯丙烯的方法 | |
| CN119019218A (zh) | 一种用于由1,3-二氯丙烯和3-氯丙烯混合制备1,1,2,3-四氯丙烯的方法 | |
| US3949009A (en) | Process for preparing trichloroethylene | |
| CN120590302A (zh) | 硫醚的连续流氧化成砜的方法 | |
| Smolyan et al. | DEVELOPMENTS IN THE CHLORINATIONOF SATURATED HYDROCARBONS |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |