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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111021Generated: October 30, 2026

Allyl bromide → N-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea

https://huagongshe.com/reaction/1111021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium MethoxideHCID 10942334—
ReactantN-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylureaHCID 72742602—
SolventWaterHCID 962—
ProductN-[4-(1-allyloxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylureaHCID 54128761—

Reaction Steps

A solution of the N-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea 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'-isopropoxycarbonylmethylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-ca254232c13e4cf6a5976595cec640d0
Source noteuspto-grants-1990_12