Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209706Generated: October 30, 2026

Ethanethiol → Ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate

https://huagongshe.com/reaction/2209706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantEthyl 2-[[4-methoxybenzenesulfonyl](isobutyl)amino]acetateHCID 10640094—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetateHCID 10591435—

Reaction Steps

A solution of ethanethiol (15 mL) and methylene chloride (15 mL) is cooled to 0° C. Aluminum trichloride (9.62 g, 72.2 mmol) is added (the solution turns green), and the reaction is warmed to room temperature. Ethyl 2-[[4-methoxybenzenesulfonyl](isobutyl)amino]acetate (4.75 g, 14.44 mmol) is added in methylene chloride (5 mL), and the reaction is stirred for 3.5 hours at room temperature. The reaction is then slowly quenched with water, and the crude reaction is partitioned between water and methylene chloride. The aqueous layer is extracted well with methylene chloride, the combined organic layers are dried (Na2SO4), and the solvent is evaporated. The product is purified by silica gel chromatography (25% to 50% ethyl acetate/hexane) to give ethyl 2-[[4-hydroxybenzenesulfonyl](isobutyl)amino]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-f3ebab5c6d1a46a18b317043078c8469
Source noteuspto-grants-1995_10