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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217467Generated: October 29, 2026

1-Chloroethyl chloroformate → HCID 19391664, compound

https://huagongshe.com/reaction/217467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 12674336HCID 12674336—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 19391664HCID 193916646.9%

Reaction Steps

To a solution of ethyl (1-methyl-1,2,3,6-tetrahydropyridin-4-yl)acetate (2.05 g) in dichloroethane (14 mL) was added 1-chloroethyl-chloroformate (1.5 mL) at 0° C. The reaction liquid was heated and refluxed for 2.5 hours, and then concentrated under reduced pressure. The residue was dissolved in MeOH (14 mL), and heated and refluxed for 1 hour. After concentration under reduced pressure, the residue was purified by amino column chromatography (chloroform:methanol=100:0 to 80:20) to obtain ethyl 1,2,3,6-tetrahydropyridin-4-ylacetate (130 mg) as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-c8b9c99d0aa7475bb775bb1ae24e2d55
Source noteuspto-grants-2012_06