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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980168Generated: October 26, 2026

Phenacyl bromide → 5-Iodo-1-phenacylpyrimidin-2-one

https://huagongshe.com/reaction/980168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant5-Iodopyrimidin-2-olHCID 11959096—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
Product5-Iodo-1-phenacylpyrimidin-2-oneHCID 12795535—

Reaction Steps

A suspension of 5-iodopyrimidin-2-one (556 mg) and α-bromoacetophenone (533 mg) in triethylamine (0.5 ml) and ethanol (50 ml) was stirred at ambient temperature for 71/2 hours. The resulting solution was evaporated and the residue triturated with water. This product was purified by preparative thin-layer chromatography on silica before crystallisation from ethyl acetate to give the title pyrimidinone: yield 253 mg: m.p. 155°-157°: λmaxEtOH 238.5 nm (ε 23070), 340 nm (ε 2400), λinf 250 nm (ε 17160), 275 nm (ε 1780).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636509
Source datasetuspto-grants-1987_01
ORD IDord-e03a08e39a184094a14204bdf2a65dc9
Source noteuspto-grants-1987_01