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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703161Generated: October 31, 2026

Ethyl chloroformate → HCID 13377594, compound

https://huagongshe.com/reaction/1703161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 214822HCID 214822—
SolventTolueneHCID 1140—
ProductHCID 13377594HCID 13377594—

Reaction Steps

43 g 4-(2,2-dimethylindane-1-ylidene)-1-methyl-piperidine and 65 g ethyl chloroformate in 800 ml toluene are refluxed for 3 hours. After cooling, the solution is washed with 1 N hydrochloric acid and water, dried over magnesium sulfate and the toluene distilled off. The oily residue is then refluxed for 6 hours in 90 ml n-butanol and 9 g potassium hydroxide. The reaction mixture is cooled, filtered, diluted with ether and shaken out with water until neutral. The organic phase is then dried over magnesium sulfate and evaporated, to give the title compound as the hydrogenofumarate: m.p. 200°-202°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351838
Source datasetuspto-grants-1982_09
ORD IDord-d589aafac1cf4836a0c6670d16c45908
Source noteuspto-grants-1982_09