Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127483Generated: November 2, 2026

Benzene → 2,2-Dichloro-1-(1-thia-4-azaspiro[4.5]decan-4-yl)ethan-1-one

https://huagongshe.com/reaction/127483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantCysteamineHCID 6058—
ReactantDichloroacetyl chlorideHCID 6593—
ReactantCyclohexanoneHCID 7967—
SolventWaterHCID 962—
Product2,2-Dichloro-1-(1-thia-4-azaspiro[4.5]decan-4-yl)ethan-1-oneHCID 13277203—

Reaction Steps

From a boiling mixture of 9.8 g. (0.1 moles) of cyclohexanone and 7.7 g. (0.1 moles) of 2-mercaptoethylamine in 100 ml. of benzene the water formed is continuously distilled off. Boiling is continued until 1.8 ml. of water are separated. The reaction mixture is then cooled and 11 g. of a 40% aqueous sodium hydroxide solution are added followed by dropwise addition of 14.7 g. (0.1 moles) of dichloroacetyl chloride, with external salt/ice cooling. Mixture is stirred for a further two hours at room temperature and washed with aqueous hydrochloric acid solution and subsequently with water. From the neutral mixture obtained benzene is distilled off in vacuo to give 17.2 g. (0.064 moles) of a white powder. Recrystallization from absolute ethanol yields a white crystalline product melting at 149° to 151° C. The structure of the named compound can be verified by IR spectrum analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256481
Source datasetuspto-grants-1981_03
ORD IDord-c9ccf6a9241a4f148b83292be52195c3
Source noteuspto-grants-1981_03