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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307906Generated: October 30, 2026

Ethanethiol → HCID 21306325, compound

https://huagongshe.com/reaction/2307906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 21306331HCID 21306331—
SolventDichloromethaneHCID 6344—
ProductHCID 21306325HCID 2130632594.8%

Reaction Steps

A mixture of β-[[(3-methoxypheyl)sulfonyl]amino]-butanoic acid, ethyl ester (7.8 g, 25.7 mmol) and ethanethiol (8 g, 0.13 mol) in methylenechloride (200 ml) was cooled in ice-bath. Aluminum chloride (17.2 g, 0.13 mol) was added to above soultion. The reaction mixture was stirred at room temperature for 4 hours. The reaction mixture was quenched with 3N HCl (200 ml). Organic layer was separated. Aqueous layer was extracted with methylene chloride (2×100 ml). Combined organic solution was concentrated and dried to give the title compound (7 g, 94%). The material was used for the next reaction without further purification. 1H NMR (300 MHz, CD3OD) □|□d, 3H, J=6.73 Hz), 1.23 (t, 3H, J=7.11 Hz), 2.31-2.49 (m, 2H), 3.66-3.74 (m, 1H), 4.01-4.16 (m, 2H), 7.00-7.04 (m, 1H), 7.27-7.41 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833366B1
Source datasetuspto-grants-2004_12
ORD IDord-7c167ba9566444448e6f023a92910cfe
Source noteuspto-grants-2004_12