SK280457B6 - Spôsob prípravy chloridov kyselín - Google Patents

Spôsob prípravy chloridov kyselín Download PDF

Info

Publication number: SK280457B6
Authority: SK; Slovakia
Prior art keywords: formula; preparation; compound; water; group
Prior art date: 1993-10-05

Application number

SK1203-94A

Other languages

English (en)

Slovak (sk)

Other versions

SK120394A3 (en

Inventor

Michael J. Bull

John W. Cornforth

Original Assignee

Shell Internationale Research Matschappij B. V.

Priority date (The priority date 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 date listed.)

1993-10-05

Filing date

1994-10-05

Publication date

2000-02-14

1994-10-05 Application filed by Shell Internationale Research Matschappij B. V. filed Critical Shell Internationale Research Matschappij B. V.

1995-05-10 Publication of SK120394A3 publication Critical patent/SK120394A3/sk

2000-02-14 Publication of SK280457B6 publication Critical patent/SK280457B6/sk

Links

239000002253 acid Substances 0.000 title claims abstract description 4
150000001805 chlorine compounds Chemical class 0.000 title claims abstract description 4
238000000034 method Methods 0.000 title claims description 23
238000002360 preparation method Methods 0.000 title claims description 17
150000001875 compounds Chemical class 0.000 claims abstract description 27
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
229910021578 Iron(III) chloride Inorganic materials 0.000 claims abstract description 10
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims abstract description 10
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 claims abstract description 3
125000005843 halogen group Chemical group 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 8
125000001188 haloalkyl group Chemical group 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000004076 pyridyl group Chemical group 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
229910052801 chlorine Inorganic materials 0.000 abstract description 13
239000000460 chlorine Substances 0.000 abstract description 11
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 9
229910052731 fluorine Inorganic materials 0.000 abstract description 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract description 4
239000011737 fluorine Substances 0.000 abstract description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract description 3
229910052794 bromium Inorganic materials 0.000 abstract description 3
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract description 2
239000002904 solvent Substances 0.000 description 16
239000002841 Lewis acid Substances 0.000 description 12
150000007517 lewis acids Chemical class 0.000 description 12
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 11
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
239000011541 reaction mixture Substances 0.000 description 8
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical class CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 7
125000001309 chloro group Chemical group Cl* 0.000 description 7
239000000203 mixture Substances 0.000 description 7
-1 aromatic acid chlorides Chemical class 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
238000010992 reflux Methods 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical group ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
KRZCOLNOCZKSDF-UHFFFAOYSA-N 4-fluoroaniline Chemical compound NC1=CC=C(F)C=C1 KRZCOLNOCZKSDF-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
239000000706 filtrate Substances 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
125000001072 heteroaryl group Chemical group 0.000 description 3
XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical class ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
125000001153 fluoro group Chemical group F* 0.000 description 2
238000004817 gas chromatography Methods 0.000 description 2
UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 2
DCUJJWWUNKIJPH-UHFFFAOYSA-N nitrapyrin Chemical compound ClC1=CC=CC(C(Cl)(Cl)Cl)=N1 DCUJJWWUNKIJPH-UHFFFAOYSA-N 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000000047 product Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
125000000547 substituted alkyl group Chemical group 0.000 description 2
229910052723 transition metal Inorganic materials 0.000 description 2
150000003624 transition metals Chemical class 0.000 description 2
229910052727 yttrium Inorganic materials 0.000 description 2
UGEJOEBBMPOJMT-UHFFFAOYSA-N 3-(trifluoromethyl)phenol Chemical compound OC1=CC=CC(C(F)(F)F)=C1 UGEJOEBBMPOJMT-UHFFFAOYSA-N 0.000 description 1
KASGMHMVKYJQKR-UHFFFAOYSA-N 6-chloro-n-(4-fluorophenyl)pyridine-2-carboxamide Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC(Cl)=N1 KASGMHMVKYJQKR-UHFFFAOYSA-N 0.000 description 1
INDXGKMKACLIJS-UHFFFAOYSA-N 6-chloropyridine-2-carbonyl chloride Chemical compound ClC(=O)C1=CC=CC(Cl)=N1 INDXGKMKACLIJS-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
230000005526 G1 to G0 transition Effects 0.000 description 1
GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
101100311330 Schizosaccharomyces pombe (strain 972 / ATCC 24843) uap56 gene Proteins 0.000 description 1
229910004298 SiO 2 Inorganic materials 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000003302 alkenyloxy group Chemical group 0.000 description 1
125000005108 alkenylthio group Chemical group 0.000 description 1
125000004448 alkyl carbonyl group Chemical group 0.000 description 1
125000004644 alkyl sulfinyl group Chemical group 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
125000005133 alkynyloxy group Chemical group 0.000 description 1
125000005109 alkynylthio group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
229940053202 antiepileptics carboxamide derivative Drugs 0.000 description 1
229910052787 antimony Inorganic materials 0.000 description 1
WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000012824 chemical production Methods 0.000 description 1
XOYLJNJLGBYDTH-UHFFFAOYSA-M chlorogallium Chemical compound [Ga]Cl XOYLJNJLGBYDTH-UHFFFAOYSA-M 0.000 description 1
238000001816 cooling Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
239000000284 extract Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000001207 fluorophenyl group Chemical group 0.000 description 1
229910052733 gallium Inorganic materials 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000004438 haloalkoxy group Chemical group 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004811 liquid chromatography Methods 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910001507 metal halide Inorganic materials 0.000 description 1
150000005309 metal halides Chemical class 0.000 description 1
OMWWTMOLTFYGAK-UHFFFAOYSA-N n-(4-fluorophenyl)benzamide Chemical compound C1=CC(F)=CC=C1NC(=O)C1=CC=CC=C1 OMWWTMOLTFYGAK-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
101150018444 sub2 gene Proteins 0.000 description 1
239000008400 supply water Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000007704 transition Effects 0.000 description 1
229910021381 transition metal chloride Inorganic materials 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1

Classifications

- 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
- C07C63/00—Compounds having carboxyl groups bound to a carbon atoms of six-membered aromatic rings
- C07C63/04—Monocyclic monocarboxylic acids
- C07C63/06—Benzoic acid
- C07C63/10—Halides thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pyridine Compounds (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Thiazole And Isothizaole Compounds (AREA)
Food Preservation Except Freezing, Refrigeration, And Drying (AREA)

SK1203-94A 1993-10-05 1994-10-05 Spôsob prípravy chloridov kyselín SK280457B6 (sk)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP93307903		1993-10-05

Publications (2)

Publication Number	Publication Date
SK120394A3 SK120394A3 (en)	1995-05-10
SK280457B6 true SK280457B6 (sk)	2000-02-14

Family

ID=8214567

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1203-94A SK280457B6 (sk)	1993-10-05	1994-10-05	Spôsob prípravy chloridov kyselín

Country Status (22)

Country	Link
EP (1)	EP0646566B1 (de)
JP (1)	JP4101311B2 (de)
KR (1)	KR100357221B1 (de)
CN (1)	CN1050833C (de)
AT (1)	ATE160337T1 (de)
AU (1)	AU676370B2 (de)
BR (1)	BR9403998A (de)
CA (1)	CA2133612A1 (de)
CZ (1)	CZ286844B6 (de)
DE (1)	DE69406885T2 (de)
DK (1)	DK0646566T3 (de)
ES (1)	ES2110700T3 (de)
GR (1)	GR3025449T3 (de)
HK (1)	HK1005336A1 (de)
HU (1)	HU213629B (de)
IL (1)	IL111117A0 (de)
RU (1)	RU2141940C1 (de)
SG (1)	SG86305A1 (de)
SK (1)	SK280457B6 (de)
TW (1)	TW378202B (de)
UA (1)	UA27882C2 (de)
ZA (1)	ZA947672B (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CZ294098B6 (cs) *	1996-08-23	2004-10-13	Americanácyanamidácompany	Způsob přípravy chloridů azinylových kyselin
US6087506A (en) *	1997-08-19	2000-07-11	American Cyanamid Company	Preparation of hetero arylcarboxamides
TW575563B (en) *	1997-08-19	2004-02-11	American Cyanamid Co	Process for the preparation of pyridyl carboxylic amides and esters
ATE460400T1 (de) *	2005-11-07	2010-03-15	Basf Se	Verfahren zur herstellung von pyridylcarbonsäureamiden und estern

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US387226A (en) *		1888-08-07		Hose-coupling
US1557154A (en) *	1924-07-22	1925-10-13	Mathieson Alkali Works Inc	Manufacture of benzoyl chloride
JPS5843380B2 (ja) *	1977-07-15	1983-09-27	日軽化工株式会社	塩化ベンゾイルの製造法
DE2841541A1 (de) *	1978-09-23	1980-04-03	Bayer Ag	Verfahren zur herstellung von gegebenenfalls substituiertem benzoylchlorid
US4562286A (en) *	1984-11-01	1985-12-31	Occidental Chemical Corporation	Process for preparing methoxytrifluoromethylnaphthoic acid from dimethylnaphthalene
DE3723069A1 (de) *	1987-07-11	1989-01-19	Bayer Ag	5-halogen-6-amino-nikotinsaeurehalogenide, ihre herstellung und ihre verwendung
EP0447044A1 (de) *	1990-02-23	1991-09-18	Eaton Corporation	Magnetoelastischer Film und Verfahren
GB9005965D0 (en) *	1990-03-16	1990-05-09	Shell Int Research	Herbicidal carboxamide derivatives

1994
- 1994-09-30 IL IL11111794A patent/IL111117A0/xx unknown
- 1994-09-30 AT AT94307194T patent/ATE160337T1/de not_active IP Right Cessation
- 1994-09-30 ES ES94307194T patent/ES2110700T3/es not_active Expired - Lifetime
- 1994-09-30 ZA ZA947672A patent/ZA947672B/xx unknown
- 1994-09-30 SG SG9607810A patent/SG86305A1/en unknown
- 1994-09-30 AU AU74318/94A patent/AU676370B2/en not_active Ceased
- 1994-09-30 DK DK94307194.4T patent/DK0646566T3/da active
- 1994-09-30 DE DE69406885T patent/DE69406885T2/de not_active Expired - Fee Related
- 1994-09-30 EP EP94307194A patent/EP0646566B1/de not_active Expired - Lifetime
- 1994-10-04 UA UA94105886A patent/UA27882C2/uk unknown
- 1994-10-04 RU RU94035677/04A patent/RU2141940C1/ru not_active IP Right Cessation
- 1994-10-04 CA CA002133612A patent/CA2133612A1/en not_active Abandoned
- 1994-10-05 JP JP26624194A patent/JP4101311B2/ja not_active Expired - Fee Related
- 1994-10-05 HU HU9402858A patent/HU213629B/hu not_active IP Right Cessation
- 1994-10-05 SK SK1203-94A patent/SK280457B6/sk unknown
- 1994-10-05 KR KR1019940025458A patent/KR100357221B1/ko not_active Expired - Fee Related
- 1994-10-05 CN CN94117018A patent/CN1050833C/zh not_active Expired - Fee Related
- 1994-10-05 CZ CZ19942451A patent/CZ286844B6/cs not_active IP Right Cessation
- 1994-10-05 BR BR9403998A patent/BR9403998A/pt not_active IP Right Cessation
- 1994-11-03 TW TW083110136A patent/TW378202B/zh not_active IP Right Cessation
1997
- 1997-11-20 GR GR970401988T patent/GR3025449T3/el unknown
1998
- 1998-05-13 HK HK98104129A patent/HK1005336A1/en not_active IP Right Cessation

Also Published As

Publication number	Publication date
IL111117A0 (en)	1994-11-28
HU213629B (en)	1997-08-28
DE69406885D1 (de)	1998-01-02
CN1050833C (zh)	2000-03-29
JP4101311B2 (ja)	2008-06-18
CA2133612A1 (en)	1995-04-06
DE69406885T2 (de)	1998-04-09
AU676370B2 (en)	1997-03-06
JPH07258147A (ja)	1995-10-09
ATE160337T1 (de)	1997-12-15
TW378202B (en)	2000-01-01
EP0646566A1 (de)	1995-04-05
RU94035677A (ru)	1996-09-10
BR9403998A (pt)	1995-06-13
HUT69030A (en)	1995-08-28
AU7431894A (en)	1995-04-27
DK0646566T3 (da)	1997-12-22
KR100357221B1 (ko)	2003-03-03
KR950011393A (ko)	1995-05-15
HU9402858D0 (en)	1995-01-30
UA27882C2 (uk)	2000-10-16
CZ245194A3 (en)	1995-10-18
CN1109876A (zh)	1995-10-11
ES2110700T3 (es)	1998-02-16
EP0646566B1 (de)	1997-11-19
SK120394A3 (en)	1995-05-10
SG86305A1 (en)	2002-02-19
RU2141940C1 (ru)	1999-11-27
ZA947672B (en)	1995-06-29
CZ286844B6 (en)	2000-07-12
HK1005336A1 (en)	1998-12-31
GR3025449T3 (en)	1998-02-27

Publication	Publication Date	Title
EP1277726B1 (de)	2007-01-03	Verfahren zur herstellung von 2-halobenzoesäuren
AU767603B2 (en)	2003-11-20	New process for preparing pesticidal intermediates
KR100357221B1 (ko)	2003-03-03	산클로라이드화합물의제조방법
HK1005336B (en)	1998-12-31	Process for the preparation of acid chloride compounds
US5639888A (en)	1997-06-17	Process for the preparation of acid chloride compounds
EP0899262B1 (de)	2005-04-06	Verfahren zur Herstellung von Heteroarylcarbonsäureamiden und -estern
US6087506A (en)	2000-07-11	Preparation of hetero arylcarboxamides
JP4251508B2 (ja)	2009-04-08	酸塩化物化合物の製造方法
JPH04270248A (ja)	1992-09-25	ベンジルフェニルケトン誘導体
US4374067A (en)	1983-02-15	Intermediates for the preparation of 4-phenyl-1,3-benzodiazepins and methods for preparing the intermediates
JPH0586387B2 (de)	1993-12-10
JP4427988B2 (ja)	2010-03-10	ビアリール化合物の製造方法
EP0143628B1 (de)	1989-10-11	Verfahren zur Herstellung von Salicylamidverbindungen
JP3646223B2 (ja)	2005-05-11	求電子反応による芳香族化合物の製造方法及び芳香族化合物
JPH05201955A (ja)	1993-08-10	殺生物剤化合物の製造方法
JP3486669B2 (ja)	2004-01-13	テトラアミノ化合物及びその製造方法
CZ289774B6 (cs)	2002-04-17	Způsob výroby arylamidů heteroaromatických karboxylových kyselin
JP2540167B2 (ja)	1996-10-02	マレイミドの製造方法
JPH0713041B2 (ja)	1995-02-15	ハロゲノニトロベンゼン誘導体とその製造方法
KR20000052892A (ko)	2000-08-25	나프티리딘 화합물의 제조 방법 및 신규 중간 생성물
HUP9904291A2 (hu)	2000-05-28	Eljárás naftiridinvegyületek előállítására, és az új köztitermékek
HK1018060B (en)	2005-08-26	Process for the preparation of heteroarylcarboxylic amides and esters
JPH01180876A (ja)	1989-07-18	ピリジン化合物
JPS6323823A (ja)	1988-02-01	アミド化合物の製造方法