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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382486Generated: November 1, 2026

Formamidine → (4-Chlorophenyl)(pyrimidin-5-yl)methanone

https://huagongshe.com/reaction/1382486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidineHCID 68047—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantHCID 3456926HCID 3456926—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(4-Chlorophenyl)(pyrimidin-5-yl)methanoneHCID 1364565231%

Reaction Steps

7.7 g (0.065 mole) of N,N-dimethylformamide dimethyl acetal are added in portions to 10 g (0.055 mole) of 4-chlorophenyl hydroxyvinyl ketone (compare 1st stage) in 10 ml of toluene at 0° C. The reaction mixture is subsequently stirred for 15 minutes, and 5.7 g (0.055 mole) of formamidine kacetate are then added. After further subsequent stirring for 15 minutes, a solution of 3 g (0.055 mole) of sodium methylate in 80 ml of ethanol is added dropwise and the mixture is subsequently stirred under reflux for 8 hours. The reaction mixture is allowed to cool and is poured onto 400 ml of water and extracted with toluene. The organic phase is washed with water, dried over sodium sulphate and concentrated. The residue is purified by column chromatography (ethyl acetate: cyclohexane=3:1; silica gel). 3.7 g (31% of theory) of 4-chlorophenyl 5-pyrimidinyl ketone of melting point 110°-112° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806644
Source datasetuspto-grants-1989_02
ORD IDord-bebe8aeec0584401bd9288c78aa0f829
Source noteuspto-grants-1989_02