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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906150Generated: October 27, 2026

5-Chloro-2(1H)-pyrimidinone → 5-Chloro-1-(3-furoylmethyl)pyrimidin-2-one

https://huagongshe.com/reaction/1906150

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2(1H)-pyrimidinoneHCID 108578—
Reactant3-BromoacetylfuranHCID 18612551—
SolventEthanolHCID 702—
SolventTriethylamineHCID 8471—
Product5-Chloro-1-(3-furoylmethyl)pyrimidin-2-oneHCID 1279124431.2%

Reaction Steps

A mixture of 5-chloropyrimidin-2-one (587 mg) and crude 3-bromoacetylfuran (2.00 g, ca. 4.5 mmol, based on purity ca. 40% by 1H n.m.r; contaminated with 3-dibromoacetylfuran and diethyl ether) in triethylamine (0.95 ml) and ethanol (25 ml) was stirred at room temperature. After 45 min with solvent was removed and the residue triturated with ethyl acetate. The resulting solid was collected and retriturated with water. This gave a buff solid which was crystallised from ethyl acetate to give the title pyrimidinone (335 mg), m.p. 195°-197° C. (dec), λmax (EtOH) 333 nm (ε 2,530).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04650800
Source datasetuspto-grants-1987_03
ORD IDord-6e8a7b94c0684666a0c46504021d0e00
Source noteuspto-grants-1987_03