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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903004Generated: October 25, 2026

Allyl chloride → Ethyl [(prop-2-en-1-yl)oxy]carbamate

https://huagongshe.com/reaction/903004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantHydroxyurethaneHCID 11510—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
ProductEthyl [(prop-2-en-1-yl)oxy]carbamateHCID 19860187—

Reaction Conditions

Temperature80 °C

Reaction Steps

100 g of N-hydroxyurethane and 80.3 g of allyl chloride were added, at 20° C., to a solution of 53.8 g of potassium hydroxide in 750 ml of ethanol. The mixture was stirred and refluxed (80° C.) for 4 hours, then was cooled to 25° C. and filtered. The solvent was evaporated from the filtrate and the residue, an oil, was distilled, 51°-55° C., 0.2 Torr., to give ethyl (2-propenyloxy)carbamate, 3A, as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04226612
Source datasetuspto-grants-1980_10
ORD IDord-0eda31aec55b414b8acdd83dfd38cd52
Source noteuspto-grants-1980_10