Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 980184Generated: October 30, 2026

Bromomethyl 3-methoxyphenyl ketone → HCID 12795559, compound

https://huagongshe.com/reaction/980184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 3-methoxyphenyl ketoneHCID 101294—
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
ProductHCID 12795559HCID 1279555920.5%

Reaction Steps

A solution of 5-chloropyrimidin-2-one (504 mg) and 2-bromo-3'-methoxyacetophenone (880 mg) in triethylamine (1 ml) and ethanol (50 ml) was stirred at ambient temperature for 20 hours. After evaporation of solvents, the residue was triturated with water (50 ml). The resulting solid was crystallised from ethyl acetate to give the title pyrimidinone (220 mg,); m.p. 134°-137°; λmaxEtOH 249.5 nm (ε 12660), 317 nm (ε 4070), λinf 334.5 nm (ε2950), 344.5 nm (ε 1990).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04636509
Source datasetuspto-grants-1987_01
ORD IDord-5647dcf55a024fa3b167822552d9ed9e
Source noteuspto-grants-1987_01