JPS6215048B2 - - Google Patents
Info
- Publication number
- JPS6215048B2 JPS6215048B2 JP54055180A JP5518079A JPS6215048B2 JP S6215048 B2 JPS6215048 B2 JP S6215048B2 JP 54055180 A JP54055180 A JP 54055180A JP 5518079 A JP5518079 A JP 5518079A JP S6215048 B2 JPS6215048 B2 JP S6215048B2
- Authority
- JP
- Japan
- Prior art keywords
- chlorine
- azo
- bis
- reaction
- methyl chloride
- 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
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 claims abstract description 51
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims abstract description 39
- 238000006243 chemical reaction Methods 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 26
- 239000003999 initiator Substances 0.000 claims abstract description 24
- 229940050176 methyl chloride Drugs 0.000 claims abstract description 23
- 150000008049 diazo compounds Chemical class 0.000 claims abstract description 8
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 239000007791 liquid phase Substances 0.000 claims abstract description 3
- 239000000460 chlorine Substances 0.000 claims description 35
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 29
- 229910052801 chlorine Inorganic materials 0.000 claims description 29
- 239000011541 reaction mixture Substances 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 238000007348 radical reaction Methods 0.000 claims description 5
- 150000003254 radicals Chemical class 0.000 claims description 5
- VXVUDUCBEZFQGY-UHFFFAOYSA-N 4,4-dimethylpentanenitrile Chemical compound CC(C)(C)CCC#N VXVUDUCBEZFQGY-UHFFFAOYSA-N 0.000 claims description 2
- 238000010494 dissociation reaction Methods 0.000 claims description 2
- 230000005593 dissociations Effects 0.000 claims description 2
- 238000005660 chlorination reaction Methods 0.000 abstract description 8
- -1 peroxide compounds Chemical class 0.000 abstract description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 12
- 238000002474 experimental method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 7
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 2
- YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 229910001447 ferric ion Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- ICBDEAIMBSLBPZ-UHFFFAOYSA-N (2,4-dinitrophenyl)-trityldiazene Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC=C1N=NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 ICBDEAIMBSLBPZ-UHFFFAOYSA-N 0.000 description 1
- INKOVEUKFFRUDP-UHFFFAOYSA-N (4-bromophenyl)-trityldiazene Chemical compound C1=CC(Br)=CC=C1N=NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 INKOVEUKFFRUDP-UHFFFAOYSA-N 0.000 description 1
- DIKSUAXFQBITOE-UHFFFAOYSA-N (4-methylphenyl)-trityldiazene Chemical compound C1=CC(C)=CC=C1N=NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 DIKSUAXFQBITOE-UHFFFAOYSA-N 0.000 description 1
- ZRSLOTOZLGLTSX-UHFFFAOYSA-N (4-nitrophenyl)-trityldiazene Chemical compound C1=CC([N+](=O)[O-])=CC=C1N=NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 ZRSLOTOZLGLTSX-UHFFFAOYSA-N 0.000 description 1
- IWCFQILSJWBEOS-UHFFFAOYSA-N 1-[(1-cyanocyclododecyl)diazenyl]cyclododecane-1-carbonitrile Chemical compound C1CCCCCCCCCCC1(C#N)N=NC1(C#N)CCCCCCCCCCC1 IWCFQILSJWBEOS-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- UFDMOVHWSRRBHX-UHFFFAOYSA-N 3,7-diphenyl-4,5,6,7-tetrahydro-3h-diazepine Chemical compound C1CCC(C=2C=CC=CC=2)N=NC1C1=CC=CC=C1 UFDMOVHWSRRBHX-UHFFFAOYSA-N 0.000 description 1
- HPUSHAOHRBOVMT-UHFFFAOYSA-N 4-(trityldiazenyl)phenol Chemical compound OC1=CC=C(C=C1)N=NC(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1 HPUSHAOHRBOVMT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QJIKPFOHBCRSAY-UHFFFAOYSA-N bis(1-propan-2-ylcyclohexa-2,4-dien-1-yl)diazene Chemical compound C1C=CC=CC1(C(C)C)N=NC1(C(C)C)CC=CC=C1 QJIKPFOHBCRSAY-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- RRQDOXSDGSRAFK-UHFFFAOYSA-N chloromethane Chemical compound ClC.ClC RRQDOXSDGSRAFK-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000007038 hydrochlorination reaction Methods 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- FBBDOOHMGLLEGJ-UHFFFAOYSA-N methane;hydrochloride Chemical compound C.Cl FBBDOOHMGLLEGJ-UHFFFAOYSA-N 0.000 description 1
- KWWXJMQHDYEIQS-UHFFFAOYSA-N n-[4-(trityldiazenyl)phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1N=NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 KWWXJMQHDYEIQS-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- YFMFSCRSAWIWOP-UHFFFAOYSA-N phenyl(trityl)diazene Chemical compound C1=CC=CC=C1N=NC(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 YFMFSCRSAWIWOP-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Glass Compositions (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR7813601A FR2424893A1 (fr) | 1978-05-05 | 1978-05-05 | Procede pour la fabrication de dichloromethane |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54145602A JPS54145602A (en) | 1979-11-14 |
JPS6215048B2 true JPS6215048B2 (US07655746-20100202-C00011.png) | 1987-04-06 |
Family
ID=9208000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5518079A Granted JPS54145602A (en) | 1978-05-05 | 1979-05-04 | Manufacture of methylene chloride |
Country Status (6)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62165146U (US07655746-20100202-C00011.png) * | 1986-04-10 | 1987-10-20 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4614572A (en) * | 1985-07-08 | 1986-09-30 | The Dow Chemical Company | Liquid phase chlorination of chlorinated methanes |
JP4849811B2 (ja) * | 2004-05-31 | 2012-01-11 | 株式会社トクヤマ | 高次塩素化メタン類の製造方法 |
WO2013096311A1 (en) * | 2011-12-22 | 2013-06-27 | Dow Global Technologies, Llc | Process for the production of tetrachloromethane |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4924886A (US07655746-20100202-C00011.png) * | 1972-07-03 | 1974-03-05 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB489554A (en) * | 1936-01-29 | 1938-07-28 | Ig Farbenindustrie Ag | Manufacture of higher chlorinated methanes |
FR894906A (fr) * | 1942-05-30 | 1945-01-10 | Ig Farbenindustrie Ag | Procédé pour préparer des hydrocarbures chlorés |
US2715146A (en) * | 1949-06-01 | 1955-08-09 | British Celanese | Process and catalyst for methylene chloride production |
DE2106886C3 (de) * | 1970-03-12 | 1985-03-21 | Solvay & Cie., Brüssel/Bruxelles | Verfahren zur Herstellung von Methylenchlorid durch thermische Chlorierung von Methan |
BE812043A (fr) * | 1974-03-08 | 1974-07-01 | Procede de fabrication de 1 |
-
1978
- 1978-05-05 FR FR7813601A patent/FR2424893A1/fr active Granted
-
1979
- 1979-05-02 AT AT79200205T patent/ATE536T1/de not_active IP Right Cessation
- 1979-05-02 EP EP79200205A patent/EP0005296B1/fr not_active Expired
- 1979-05-02 DE DE7979200205T patent/DE2961745D1/de not_active Expired
- 1979-05-04 JP JP5518079A patent/JPS54145602A/ja active Granted
- 1979-05-04 ES ES480231A patent/ES480231A1/es not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4924886A (US07655746-20100202-C00011.png) * | 1972-07-03 | 1974-03-05 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62165146U (US07655746-20100202-C00011.png) * | 1986-04-10 | 1987-10-20 |
Also Published As
Publication number | Publication date |
---|---|
DE2961745D1 (en) | 1982-02-25 |
FR2424893B1 (US07655746-20100202-C00011.png) | 1980-10-10 |
FR2424893A1 (fr) | 1979-11-30 |
JPS54145602A (en) | 1979-11-14 |
EP0005296B1 (fr) | 1982-01-06 |
EP0005296A1 (fr) | 1979-11-14 |
ATE536T1 (de) | 1982-01-15 |
ES480231A1 (es) | 1980-02-01 |
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