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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720616Generated: October 26, 2026

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

https://huagongshe.com/reaction/1720616

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 numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-dbdfa12401ae41769e6acfc891c1a4b1
Source noteuspto-grants-1996_04