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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111008Generated: October 29, 2026

2-Butene, 1-bromo- → N'-n-propoxycarbonylmethylurea

https://huagongshe.com/reaction/1111008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butene, 1-bromo-HCID 122414—
ReactantSodium MethoxideHCID 10942334—
ReactantN-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylureaHCID 86744397—
SolventWaterHCID 962—
ProductN'-n-propoxycarbonylmethylureaHCID 86744398—

Reaction Steps

A solution of N-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylurea in 25% methanolic sodium methoxide (1.0 equivalent) is treated at room temperature with 1.1 equivalent of crotyl 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-crotyloxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-f525c65173264ad0a2ed900b37418fc2
Source noteuspto-grants-1990_12