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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27423Generated: October 25, 2026

Water → 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepine

https://huagongshe.com/reaction/27423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl (4-chlorophenyl)acetateHCID 84177—
ReactantSodiumHCID 5360545—
ReactantHCID 178483040HCID 178483040—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepineHCID 53941548—

Reaction Steps

Add (drop by drop at 90° in a stream of nitrogen to let the alcohol escape) a solution of 4.6 g of sodium in 100 ml of ethyl alcohol to a mixture of 53.2 g of the title compound of Example 1 and 29.8 g of ethyl 4-chlorophenylacetate. Stir it for a further 4 hours at 90° and then cool it to ambient temperature. Mix the cooled reaction mixture with 100 ml of water and 100 ml of diethyl ether, collect the organic phase and dry the latter over sodium sulfate. Concentrate the dried organic phase and then distil off any excess ethyl 4-chlorophenylacetate under a high vacuum to obtain a crude yield [15.5 g (34% of theory)] of the title compound as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04221788
Source datasetuspto-grants-1980_09
ORD IDord-ca593dee24784df38759aae09bcc0859
Source noteuspto-grants-1980_09