Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358436Generated: October 26, 2026

p-Chlorothiophenol → 3-[(4-Chlorophenyl)thio]-azacycloheptan-2-one

https://huagongshe.com/reaction/358436

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ChlorothiophenolHCID 7815—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Bromoazepan-2-oneHCID 11030635—
SolventMethanolHCID 887—
Product3-[(4-Chlorophenyl)thio]-azacycloheptan-2-oneHCID 13268904—

Reaction Steps

54 g (1.0 mol) of sodium methylate and 144.6 g (1.0 mol) of 4-chlorothiophenol are initially introduced into 500 mL of methanol, and a methanolic solution of 192 g (1.0 mol) of α-bromocaprolactam is added dropwise at room temperature. After the exothermic reaction has ceased, the mixture is stirred for a further 3 hours at room temperature, the precipitated sodium bromide is then filtered off under suction and the mother liquor is evaporated down in vacuo. The precipitated crystals are filtered off under suction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04468392
Source datasetuspto-grants-1984_08
ORD IDord-c7b72039f4ed450ca9110350fd3d7b5e
Source noteuspto-grants-1984_08