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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271090Generated: November 2, 2026

Allylamine → benzyl N-(prop-2-en-1-yl)carbamate

https://huagongshe.com/reaction/1271090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
SolventDichloromethaneHCID 6344—
Productbenzyl N-(prop-2-en-1-yl)carbamateHCID 562279—

Reaction Steps

To a solution of allylamine (58 mmoles, 3.34 g) at 0° C. in dichloromethane (100 mL) was added triethylamine (120 mmoles, 16 mL). The mixture was stirred for two minutes, then benzylchloroformate (58 mmoles, 8.25 mL) added dropwise. The resulting solution was stirred at 0° C. for 2 hours, and at ambient temperature for an additional 90 minutes. A white precipitate formed, which was filtered off. Solvent was removed from the filtrate under reduced pressure, and the residue chromatographed on a silica gel column, eluting with 20% ethyl acetate/hexanes, to give benzyl allylcarbamate, a compound of formula (2), as a clear oil. Yield: 5.0 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205303B2
Source datasetuspto-grants-2007_04
ORD IDord-75604d7187b147318690301055b9be17
Source noteuspto-grants-2007_04