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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916659Generated: October 27, 2026

Triethylamine → Ethyl 4-(4-bromo-phenylsulphanyl)-5-oxo-azepan-1-carboxylate

https://huagongshe.com/reaction/1916659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-BromothiophenolHCID 66049—
ReactantEthyl 4-bromo-5-oxo-azepan-1-carboxylateHCID 69077672—
SolventChloroformHCID 6212—
ProductEthyl 4-(4-bromo-phenylsulphanyl)-5-oxo-azepan-1-carboxylateHCID 69076506—

Reaction Steps

60.5 g (320 mmol) 4-bromothiophenol in 300 mL chloroform are added to a solution of 84.5 g (320 mmol) ethyl 4-bromo-5-oxo-azepan-1-carboxylate and 32.4 g (320 mmol) triethylamine in 80 mL chloroform over 45 min, so that the internal temperature does not exceed 40° C. The reaction solution is stirred for 1.5 h at RT. The reaction mixture is washed twice with dilute ammonia solution and twice with water. The organic phase is dried over Na2SO4 and K2CO3 and the solvent is eliminated i.vac. The purification is carried out by repeated column chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-4ec93c4ee9ec4c0fb81cb1ce5a720628
Source noteuspto-grants-2013_12