JPH0557249B2 - - Google Patents
Info
- Publication number
- JPH0557249B2 JPH0557249B2 JP3151064A JP15106491A JPH0557249B2 JP H0557249 B2 JPH0557249 B2 JP H0557249B2 JP 3151064 A JP3151064 A JP 3151064A JP 15106491 A JP15106491 A JP 15106491A JP H0557249 B2 JPH0557249 B2 JP H0557249B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- acid
- reaction
- dimethyl
- 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 - Lifetime
Links
- 238000006243 chemical reaction Methods 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 16
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical class O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 10
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- 239000002841 Lewis acid Substances 0.000 claims description 4
- 150000007517 lewis acids Chemical class 0.000 claims description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 claims 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 31
- 150000001875 compounds Chemical class 0.000 description 24
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 16
- 239000011541 reaction mixture Substances 0.000 description 13
- 229910052801 chlorine Inorganic materials 0.000 description 12
- 239000000460 chlorine Substances 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- 238000009835 boiling Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- 229940098779 methanesulfonic acid Drugs 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- 238000004508 fractional distillation Methods 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- LBHGSAKAIUSJGR-UHFFFAOYSA-N 1,1,5,5-tetrachloro-3,3-dimethylpent-1-ene Chemical compound ClC(Cl)CC(C)(C)C=C(Cl)Cl LBHGSAKAIUSJGR-UHFFFAOYSA-N 0.000 description 3
- AXOLUEXMIKZJNV-UHFFFAOYSA-N 1,1,5-trichloro-3,3-dimethylpent-1-ene Chemical compound ClCCC(C)(C)C=C(Cl)Cl AXOLUEXMIKZJNV-UHFFFAOYSA-N 0.000 description 3
- JOYMMGLWENYDCV-UHFFFAOYSA-N 2,5,5-trichloro-3,3-dimethylpentanoyl chloride Chemical compound ClC(Cl)CC(C)(C)C(Cl)C(Cl)=O JOYMMGLWENYDCV-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000004566 IR spectroscopy Methods 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- CEVQMSNVKOEJQE-UHFFFAOYSA-N 1,1,1,3-tetrachloro-3-methylbutane Chemical compound CC(C)(Cl)CC(Cl)(Cl)Cl CEVQMSNVKOEJQE-UHFFFAOYSA-N 0.000 description 2
- VOKJAXLHHKZFCO-UHFFFAOYSA-N 1,1-dichloro-5-fluoro-3,3-dimethylpent-1-ene Chemical compound FCCC(C)(C)C=C(Cl)Cl VOKJAXLHHKZFCO-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- SDBFJXPUVPZONK-UHFFFAOYSA-N ClCC(C(Cl)(Cl)Cl)(C)C Chemical compound ClCC(C(Cl)(Cl)Cl)(C)C SDBFJXPUVPZONK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 230000002140 halogenating effect Effects 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- PTQGFDXPHNRDCV-CRCLSJGQSA-N (1s,3s)-3-formyl-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)[C@@H](C=O)[C@@H]1C(O)=O PTQGFDXPHNRDCV-CRCLSJGQSA-N 0.000 description 1
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- -1 1,1,5-trichloro-3,3-dimethyl-pentyl Chemical group 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- PKRFQAWEVJJQIE-UHFFFAOYSA-N 1,1-dichloro-3,3-dimethylbut-1-ene Chemical compound CC(C)(C)C=C(Cl)Cl PKRFQAWEVJJQIE-UHFFFAOYSA-N 0.000 description 1
- FWWDARKGGUNRPN-UHFFFAOYSA-N 1,1-dichloro-3-methylbut-1-ene Chemical compound CC(C)C=C(Cl)Cl FWWDARKGGUNRPN-UHFFFAOYSA-N 0.000 description 1
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 1
- QGCOTJZDMVMLRQ-UHFFFAOYSA-N 1,3-dichloro-3-methylbutane Chemical compound CC(C)(Cl)CCCl QGCOTJZDMVMLRQ-UHFFFAOYSA-N 0.000 description 1
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- IYNSGSISWKADME-UHFFFAOYSA-N 2,5,5-trichloro-3,3-dimethylpentanoic acid Chemical compound ClC(Cl)CC(C)(C)C(Cl)C(O)=O IYNSGSISWKADME-UHFFFAOYSA-N 0.000 description 1
- NBYOWTRRGFIQJJ-UHFFFAOYSA-N 2,5-dichloro-2-ethyl-3,3-dimethylpentanoic acid Chemical compound CCC(Cl)(C(O)=O)C(C)(C)CCCl NBYOWTRRGFIQJJ-UHFFFAOYSA-N 0.000 description 1
- SLKIANBIVOVBBO-UHFFFAOYSA-N 2,5-dichloro-3,3-dimethylpentanoic acid Chemical compound ClCCC(C)(C)C(Cl)C(O)=O SLKIANBIVOVBBO-UHFFFAOYSA-N 0.000 description 1
- HQXYGCABIWRICJ-UHFFFAOYSA-N 2,5-dichloro-3,3-dimethylpentanoyl chloride Chemical compound ClCCC(C)(C)C(Cl)C(Cl)=O HQXYGCABIWRICJ-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- DSJWOLVWBVIHRB-UHFFFAOYSA-N 2-bromo-3,3-dimethylbutanoyl chloride Chemical compound CC(C)(C)C(Br)C(Cl)=O DSJWOLVWBVIHRB-UHFFFAOYSA-N 0.000 description 1
- HJJGLVMKXXFRIG-UHFFFAOYSA-N 2-bromo-5,5-dichloro-3,3-dimethylpentanoic acid Chemical compound ClC(Cl)CC(C)(C)C(Br)C(O)=O HJJGLVMKXXFRIG-UHFFFAOYSA-N 0.000 description 1
- PTMTZYWRBJHXOH-UHFFFAOYSA-N 2-chloro-5-fluoro-3,3-dimethylpentanoic acid Chemical compound FCCC(C)(C)C(Cl)C(O)=O PTMTZYWRBJHXOH-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 229910003074 TiCl4 Inorganic materials 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- PQLAYKMGZDUDLQ-UHFFFAOYSA-K aluminium bromide Chemical compound Br[Al](Br)Br PQLAYKMGZDUDLQ-UHFFFAOYSA-K 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- HMPHJJBZKIZRHG-UHFFFAOYSA-N chloromethanesulfonic acid Chemical compound OS(=O)(=O)CCl HMPHJJBZKIZRHG-UHFFFAOYSA-N 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 1
- 229940008406 diethyl sulfate Drugs 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 1
- WNFUWONOILPKNX-UHFFFAOYSA-N ethyl 2-bromo-3-methylbutanoate Chemical compound CCOC(=O)C(Br)C(C)C WNFUWONOILPKNX-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003470 sulfuric acid monoesters Chemical class 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 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
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/208—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being MX
-
- 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
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/269—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions of only halogenated hydrocarbons
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/58—Preparation of carboxylic acid halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
- C07C53/19—Acids containing three or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
- C07C53/19—Acids containing three or more carbon atoms
- C07C53/21—Acids containing three or more carbon atoms containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/38—Acyl halides
- C07C53/46—Acyl halides containing halogen outside the carbonyl halide group
- C07C53/50—Acyl halides containing halogen outside the carbonyl halide group of acids containing three or more carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813111848 DE3111848A1 (de) | 1981-03-26 | 1981-03-26 | Verfahren zur herstellung von substituierten (alpha)-halogen-propionsaeuren und ihren derivaten |
| DE3111848.8 | 1981-03-26 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57045736A Division JPS57169442A (en) | 1981-03-26 | 1982-03-24 | Substituted alpha-halogenopropionic acid, derivatives thereof and manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05975A JPH05975A (ja) | 1993-01-08 |
| JPH0557249B2 true JPH0557249B2 (en]) | 1993-08-23 |
Family
ID=6128296
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57045736A Granted JPS57169442A (en) | 1981-03-26 | 1982-03-24 | Substituted alpha-halogenopropionic acid, derivatives thereof and manufacture |
| JP3151064A Granted JPH05975A (ja) | 1981-03-26 | 1991-05-27 | 置換塩化ビニリデン及びその製造方法 |
| JP3149278A Granted JPH04330038A (ja) | 1981-03-26 | 1991-05-27 | 置換α−ハロゲノプロピオン酸 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57045736A Granted JPS57169442A (en) | 1981-03-26 | 1982-03-24 | Substituted alpha-halogenopropionic acid, derivatives thereof and manufacture |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3149278A Granted JPH04330038A (ja) | 1981-03-26 | 1991-05-27 | 置換α−ハロゲノプロピオン酸 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4440947A (en]) |
| EP (1) | EP0061629B1 (en]) |
| JP (3) | JPS57169442A (en]) |
| BR (1) | BR8201735A (en]) |
| DE (2) | DE3111848A1 (en]) |
| DK (1) | DK137882A (en]) |
| HU (2) | HU186048B (en]) |
| IL (1) | IL65325A (en]) |
| ZA (1) | ZA822030B (en]) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4727181A (en) * | 1986-04-21 | 1988-02-23 | The Dow Chemical Company | Process for the preparation of α-halocinnamate esters |
| CA2144533A1 (en) * | 1992-09-22 | 1994-03-31 | Ramesh T. Talwalker | Antimicrobial composition and method of preparation |
| US5907017A (en) * | 1997-01-31 | 1999-05-25 | Cornell Research Foundation, Inc. | Semifluorinated side chain-containing polymers |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2410541A (en) * | 1942-04-10 | 1946-11-05 | Du Pont | Polyhalogenated olefins |
| US2557779A (en) * | 1946-11-07 | 1951-06-19 | Dow Chemical Co | Halogenated derivatives of aliphatic acids and method of making same |
| US2515306A (en) * | 1949-04-26 | 1950-07-18 | Us Rubber Co | Process for producing esters of omega, omega, omega-trihalo aliphatic carboxylic acids |
| BE622938A (en]) * | 1961-09-28 | |||
| FR1330693A (fr) * | 1962-08-14 | 1963-06-21 | Asahi Chemical Ind | Procédé perfectionné de production de l'acide alpha-chloroglutarique |
| US3475445A (en) * | 1965-12-03 | 1969-10-28 | Monsanto Res Corp | Halogen substituted alkenyl thiazolinylthioethers |
| US3742047A (en) * | 1969-10-27 | 1973-06-26 | Monsanto Co | Preparation of acid chlorides |
| DE2263580C2 (de) * | 1972-12-27 | 1982-06-03 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Chloracetylchlorid |
| US4053380A (en) * | 1975-04-14 | 1977-10-11 | Kurraray Co., Ltd. | 1,1,1-trihalogeno-4-methylpentenes, method of preparing the same and use of the same in the preparation of 1,1-dihalogeno-4-methyl-1,3-pentadienes |
-
1981
- 1981-03-26 DE DE19813111848 patent/DE3111848A1/de not_active Withdrawn
-
1982
- 1982-03-05 US US06/355,042 patent/US4440947A/en not_active Expired - Fee Related
- 1982-03-13 EP EP82102028A patent/EP0061629B1/de not_active Expired
- 1982-03-13 DE DE8282102028T patent/DE3276859D1/de not_active Expired
- 1982-03-23 IL IL65325A patent/IL65325A/xx unknown
- 1982-03-24 JP JP57045736A patent/JPS57169442A/ja active Granted
- 1982-03-25 DK DK137882A patent/DK137882A/da not_active Application Discontinuation
- 1982-03-25 ZA ZA822030A patent/ZA822030B/xx unknown
- 1982-03-25 HU HU82913A patent/HU186048B/hu not_active IP Right Cessation
- 1982-03-25 HU HU843363A patent/HU189429B/hu not_active IP Right Cessation
- 1982-03-26 BR BR8201735A patent/BR8201735A/pt unknown
-
1991
- 1991-05-27 JP JP3151064A patent/JPH05975A/ja active Granted
- 1991-05-27 JP JP3149278A patent/JPH04330038A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| EP0061629A3 (en) | 1983-01-26 |
| EP0061629B1 (de) | 1987-07-29 |
| ZA822030B (en) | 1983-03-30 |
| HU189429B (en) | 1986-07-28 |
| US4440947A (en) | 1984-04-03 |
| JPH04330038A (ja) | 1992-11-18 |
| IL65325A (en) | 1985-05-31 |
| JPH0526773B2 (en]) | 1993-04-19 |
| DE3276859D1 (en) | 1987-09-03 |
| HU186048B (en) | 1985-05-28 |
| BR8201735A (pt) | 1983-02-22 |
| JPS57169442A (en) | 1982-10-19 |
| DE3111848A1 (de) | 1982-10-14 |
| JPH0369895B2 (en]) | 1991-11-05 |
| JPH05975A (ja) | 1993-01-08 |
| DK137882A (da) | 1982-09-27 |
| IL65325A0 (en) | 1982-05-31 |
| EP0061629A2 (de) | 1982-10-06 |
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