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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111022Generated: October 31, 2026

Allyl bromide → HCID 53694034, compound

https://huagongshe.com/reaction/1111022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86742134HCID 86742134—
SolventWaterHCID 962—
ProductHCID 53694034HCID 53694034—

Reaction Steps

A solution of the N-[4-(1-hydroxyiminoethyl)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 product N-[4-(1-allyloxyiminoethyl)phenyl]-N'-tert-butoxycarbonylmethylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-dd44bea3c7c5441ca1bcbd84ea6327e4
Source noteuspto-grants-1990_12