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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075177Generated: October 26, 2026

Homoallyl bromide → 1-(3-Butenyl)-5-bromopyrimid-2-one

https://huagongshe.com/reaction/1075177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoallyl bromideHCID 21241—
Reactant5-Bromo-2(1H)-pyrimidinoneHCID 101494—
ReactantPotassiumHCID 5462222—
SolventMethanolHCID 887—
Product1-(3-Butenyl)-5-bromopyrimid-2-oneHCID 2049429650%

Reaction Steps

A mixture of the potassium salt of 5-bromopyrimid-2-one (0.01 mol) and 4-bromo-1-butene (0.015 mol) was heated in methanol (60 ml) at 70° C. for 40 h. The reaction mixture was then evaporated and the mixture extracted with chloroform. This solution was washed with 1 N NaOH (5 ml). with water (5 ml) and dried (MgSO4) before evaporating; yield 50%, m.p. 127°-128° C. (acetone). (Found: C, 42.06; H, 3.94. Calc. for C8H9BrN2O: C, 41.94; H, 3.96).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395406
Source datasetuspto-grants-1983_07
ORD IDord-c827da2bd0484d6e871f7e697a2c3aef
Source noteuspto-grants-1983_07