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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275030Generated: October 31, 2026

1-Chloroethyl chloroformate → HCID 53811449, compound

https://huagongshe.com/reaction/275030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 3072058HCID 3072058—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 53811449HCID 53811449140%

Reaction Steps

A solution of 13.2 g of 1-benzyl-1,2,5,6-tetrahydropyridin-3-carboxaldehyde-O-methyloxime in 120 cm3 of anhydrous 1,2-dichloroethane is cooled to 0° C., 11.7 g of alpha-chloroethyl-chloroformate is added and the whole is heated to reflux for 2 hours. After cooling, the insoluble matter is filtered off. The filtrate is evaporated to dryness, and the residue is taken up with anhydrous ether, diluted and filtered. The filtrate is evaporated and 19.8 g of product is obtained which is used immediately for the following reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391754
Source datasetuspto-grants-1995_02
ORD IDord-dbdbfcfe59584b45b2645069b73d3c1c
Source noteuspto-grants-1995_02