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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344692Generated: October 28, 2026

1-Chloroethyl chloroformate → HCID 67925064, compound

https://huagongshe.com/reaction/344692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantHCID 54089363HCID 54089363—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 67925064HCID 6792506446.2%

Reaction Steps

4 g of 1-methyl-3-(oxazol-2-yl)-1,2,5,6-tetrahydropyridine in 80 cm3 of dichloroethane is cooled to -5° C. under inert atmosphere and 3.88 g of alpha-chloroethyl chloroformate is added. The mixture is heated under reflux for one hour 30 minutes, evaporated, the residue is taken up in diethylether, followed by filtering. The ethereal phase is concentrated, the residue is taken up in 30 cm3 of methanol, heated at boiling point for 40 minutes and evaporated to dryness. After crystallization from ethanol and ether, 2.1 g of expected product is obtained. M.p.=188°-191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053416
Source datasetuspto-grants-1991_10
ORD IDord-c3999ac39aff44b39e3417f323a8222e
Source noteuspto-grants-1991_10