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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127482Generated: October 29, 2026

Benzene → 2,2-Dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone

https://huagongshe.com/reaction/127482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantEthanolamineHCID 700—
ReactantDichloroacetyl chlorideHCID 6593—
ReactantCyclohexanoneHCID 7967—
SolventWaterHCID 962—
Product2,2-Dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanoneHCID 3482402—

Reaction Steps

From a boiling mixture of 64 g. (0.645 moles) of cyclohexanone and 30 g. (0.491 moles) of ethanolamine in 100 ml. of benzene the water formed is continuously distilled off. Boiling is continued until 8.8 ml. of water are separated. The reaction mixture is then cooled, 55 g. (0.55 moles) of a 40% aqueous sodium hydroxide solution are added followed by dropwise addition of 74 g. (0.5 moles) of dichloroacetyl chloride with external salt/ice cooling. The mixture is stirred for two additional hours at room temperature and thereafter washed with an aqueous hydrochloric acid solution and subsequently with water. From the neutral mixture obtained benzene is distilled off in vacuo. 10 g. (0.4 moles) of a greenish-white crystalline substance are obtained. Recrystallization from absolute ethanol affords a white crystalline product melting at 105.5° to 107° 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-ccb974662c76495f8950a96c91e44b2d
Source noteuspto-grants-1981_03