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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742055Generated: October 26, 2026

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

https://huagongshe.com/reaction/742055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantAluminumHCID 5359268—
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 trichlofide (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 numberUS05552419
Source datasetuspto-grants-1996_09
ORD IDord-9afe8ac81c8e40299b0c193456aa3049
Source noteuspto-grants-1996_09