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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660829Generated: 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/1660829

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 numberUS08030308B2
Source datasetuspto-grants-2011_10
ORD IDord-ed296ae9e1314fc1a8963f7606fa720d
Source noteuspto-grants-2011_10