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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111014Generated: October 28, 2026

Allyl bromide → HCID 53773513, compound

https://huagongshe.com/reaction/1111014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86744400HCID 86744400—
SolventWaterHCID 962—
ProductHCID 53773513HCID 53773513—

Reaction Steps

A solution of N-[4-(hydroxyiminomethyl)phenyl]-N'-tertbutoxycarbonylmethylurea in 25% methanolic sodium methoxide (1.0 equivalent) is treated at room temperature with 1.1 equivalent of allyl bromide. The reaction mixture is stirred until the temperature falls to about 20° C. The reaction mixture is then poured into cold water and extracted with diethyl ether. The ether solution is dried over MgSO4 and filtered, and the solvent is removed by rotary evaporator to yield the corresponding N-[ 4-(allyloxyiminomethyl)phenyl]-N'-tert-butoxycarbonylmethylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-ff680108efff45e68d89f3eb01348dea
Source noteuspto-grants-1990_12