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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654461Generated: October 30, 2026

Dichloromethane → HCID 767171, compound

https://huagongshe.com/reaction/654461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
Reactant2-Amino-5-chlorobenzoic acidHCID 12476—
SolventPyridineHCID 1049—
ProductHCID 767171HCID 767171115.8%

Reaction Steps

2.0 g of 4-chlorobenzenesulfonic acid chloride are added to a solution of 3.8 g of 5-chloro-2-aminobenzoic acid [4-(3-chloro-5-trifluoromethylpyridyl-2-oxy)-anilide] in 8.6 ml of pyridine at 0° C. After the reaction mixture has been stirred for 16 hours at room temperature, 300 ml of methylene chloride are added and the resulting solution is then washed with 100 ml each of 1N HCl, H2O, saturated NaHCO3 solution and saturated NaCl solution. The organic phase is then dried with MgSO4 and concentrated by evaporation. The crude product obtained is purified by stirring in diethyl ether. In this manner 3.8 g of 5-chloro-2-[(4-chlorophenylsulfonyl)-amino]-benzoic acid [4-(3-chloro-5-trifluoromethylpyridyl-2-oxy)-anilide] are obtained in the form of white crystals (m.p. 191°-193° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05132314
Source datasetuspto-grants-1992_07
ORD IDord-c71ada4a14c344979235be517451be38
Source noteuspto-grants-1992_07