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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951537Generated: November 3, 2026

2-Chlorocyclohexanone → HCID 12696967, compound

https://huagongshe.com/reaction/1951537

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorocyclohexanoneHCID 13203—
ReactantThioacetamideHCID 2723949—
SolventEthanolHCID 702—
ProductHCID 12696967HCID 12696967—

Reaction Steps

5.00 g (37.7 mmol) of 2-chlorocyclohexanone and 2.83 g (37.7 mmol) of thioacetamide are heated in 25 ml of ethanol at the reflux temperature overnight. After cooling, the volatile components are removed in a rotary evaporator, and the remaining residue is taken up in 2 N sodium carbonate solution. It is extracted three times with dichloromethane, and the combined organic phases are dried with magnesium sulfate. The solvent is removed in a rotary evaporator, and the residue is then purified by column chromatography (silica gel, mobile phase: cyclohexane/ethyl acetate 7:3). 3.35 g (58% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404723B2
Source datasetuspto-grants-2013_03
ORD IDord-998992d07ed34be5baa5981c10b04b23
Source noteuspto-grants-2013_03