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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360279Generated: October 26, 2026

5-Chloro-2-methoxybenzene-1-sulfonyl chloride → 3-(5-Chloro-2-methoxy-benzenesulfonylamino)-4-hydroxy-5-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1360279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methoxybenzene-1-sulfonyl chlorideHCID 2734272—
Reactant3-Amino-4-hydroxy-5-trifluoromethyl-benzoic acid methyl esterHCID 66789397—
SolventTolueneHCID 1140—
Product3-(5-Chloro-2-methoxy-benzenesulfonylamino)-4-hydroxy-5-trifluoromethyl-benzoic acid methyl esterHCID 66788674—

Reaction Steps

A suspension of 3-amino-4-hydroxy-5-trifluoromethyl-benzoic acid methyl ester (4.66 g, 19.8 mmol) and 5-chloro-2-methoxybenzenesulfonyl chloride (4.78 g, 19.8 mmol) in toluene (38 mL) was heated at reflux for 48 h. After cooling, the precipitate was collected by filtration and washed with toluene to afford 3-(5-chloro-2-methoxy-benzenesulfonylamino)-4-hydroxy-5-trifluoromethyl-benzoic acid methyl ester. Off-white solid, MS (ISP)=438.0 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879845B2
Source datasetuspto-grants-2011_02
ORD IDord-5d49ab497379427bbdee1412f639e3c8
Source noteuspto-grants-2011_02