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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470208Generated: October 26, 2026

Allyl bromide → Benzyl allyl(2,2-dimethoxyethyl)carbamate

https://huagongshe.com/reaction/470208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzyl (2,2-dimethoxyethyl)carbamateHCID 10800009—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventTolueneHCID 1140—
ProductBenzyl allyl(2,2-dimethoxyethyl)carbamateHCID 1104413675.4%

Reaction Steps

A solution of benzyl N-(2,2-dimethoxyethyl)carbamate (50 g, 208.9 mmol) in toluene (180 mL) is treated with solid potassium hydroxide (51.6 g, 919.69 mmol) under nitrogen. After 10 minutes, benzyltriethylammonium chloride (0.8 g, 3.1 mmol) is added. After another 10 minutes a solution of allyl bromide (33 g, 272.8 mmol) in toluene (50 mL) is added drop wise over 10 minutes. The resultant mixture is stirred at 50° C. for 48 hours. The mixture is cooled to room temperature and quenched with water. The organic layer is separated, washed with brine, dried over magnesium sulfate, and concentrated to dryness to give the title compound (44 g, 75%). ES/MS (m/e): 280 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629270B2
Source datasetuspto-grants-2014_01
ORD IDord-932f2a05e6eb4360ac4b17c4b1a21b38
Source noteuspto-grants-2014_01