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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747592Generated: October 30, 2026

N-(4-Chloro-2-(2-chlorobenzoyl)phenyl)-3,4-dimethoxybenzenesulfonamide → N-{4-chloro-2-[(2-chlorophenyl)(hydroxy)methyl]phenyl}-3,4-dimethoxybenzenesulfonamide

https://huagongshe.com/reaction/747592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Chloro-2-(2-chlorobenzoyl)phenyl)-3,4-dimethoxybenzenesulfonamideHCID 985426—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductN-{4-chloro-2-[(2-chlorophenyl)(hydroxy)methyl]phenyl}-3,4-dimethoxybenzenesulfonamideHCID 68566152—

Reaction Steps

16 g of N-[4-chloro-2-(2-chlorobenzoyl)phenyl]-3,4-dimethoxybenzenesulfonamide dissolved in 900 ml of ethanol are added portionwise 3.93 g of sodium borohydride, and the mixture is left for 18 hours at room temperature. The reaction medium is concentrated and the residue is taken up in ethyl acetate and washed with water. The organic phase is dried over anhydrous sodium sulfate and concentrated. The residue is solidified with diisopropyl ether; after filtering off and drying the precipitate, 14.66 g of the expected product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396958B2
Source datasetuspto-grants-2008_07
ORD IDord-ac9497edd06a474a914d840599309e93
Source noteuspto-grants-2008_07