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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745436Generated: October 23, 2026

Ethyl 2-chloroacetoacetate → 5-chloro-6-methyl-1H-pyrimidin-4-one

https://huagongshe.com/en/reaction/745436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
Reactant4-MethoxybenzenecarboximidamideHCID 229074—
SolventChloroformHCID 6212—
Product5-chloro-6-methyl-1H-pyrimidin-4-oneHCID 17843321237.2%

Reaction Steps

Under N2, a solution of ethyl 2-chloroacetoacetate (1.8 ml, d=1.15, 0.013 mol) in CHCl3 (50 ml) was added dropwise to a solution 4-methoxybenzamidine (3.9 g, 0.026 mol) in CHCl3 (100 ml). After stirring overnight, the reaction mixture was filtered and the filtrate was washed with dilute NaOH solution. The aqueous layer was extracted with CH2Cl2 (3×) and the organic layer was dried, filtered and concentrated to dryness. The residue was chromatographed on silica gel and the product was eluted with 2% CH3OH-CHCl3 (v/v) to yield 0.7 g (22%) of product m.p. 250°-251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04598149
Source datasetuspto-grants-1986_07
ORD IDord-467a2c405e6b411cb6e2def6ef2ec4b7
Source noteuspto-grants-1986_07