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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896971Generated: October 29, 2026

2-Aminophenol → N-(2-hydroxyphenyl)benzenesulfonamide

https://huagongshe.com/reaction/896971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
SolventAcetoneHCID 180—
ProductN-(2-hydroxyphenyl)benzenesulfonamideHCID 23199144.2%

Reaction Steps

A flask with a stirrer was charged with 10.9 g of 2-aminophenol, 10.1 g of triethylamine and 100 ml of acetone, and a solution of 17.7 g of benzenesulfonyl chloride in 50 ml of acetone was dropwise added with cooling with ice over 30 minutes. After completion of the addition, the reaction mixture was stirred at room temperature for 2 hours and then poured into 500 ml of ice water. A precipitated crystal was recovered by filtration and washed with water. The obtained crystal was recrystallized from ethyl acetate/n-hexane mixed solvents, to give 11.0 g of an end product. Melting point 140.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921740B1
Source datasetuspto-grants-2005_07
ORD IDord-48c95e3620254e9a963d4eab7f027d0f
Source noteuspto-grants-2005_07