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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090095Generated: November 1, 2026

Dichloromethane → HCID 767171, compound

https://huagongshe.com/reaction/1090095

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 numberUS05081125
Source datasetuspto-grants-1992_01
ORD IDord-8d5b6bce266744dab7e9d7c3e1625958
Source noteuspto-grants-1992_01