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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22251Generated: October 26, 2026

4-(Trifluoromethyl)benzenecarboximidamide → 4-Methyl-2-(4-trifluoromethylphenyl)pyrimidine

https://huagongshe.com/reaction/22251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzenecarboximidamideHCID 2777390—
ReactantSodium MethoxideHCID 10942334—
Product4-Methyl-2-(4-trifluoromethylphenyl)pyrimidineHCID 1943027445.6%

Reaction Steps

To a solution of 4-trifluoromethylbenzamidine (45 g) was added sodium methoxide (11.9 g) as a solid in portions, followed by acetylaldehyde dimethylacetal (34.3 g). The mixture was refluxed overnight, then filtered, the solvent evaporated from the filtrate under reduced pressure, and the residue was partitioned between methylene chloride and water, the organic layer separated, washed with brine, dried over sodium sulfate, the solvent evaporated under reduced pressure, and the residue flash-chromatographed on silica gel, eluting with 20% ethyl acetate in heptane, to yield 13 g of 4-methyl-2-(4-trifluoromethylphenyl)pyrimidine m.p. 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428037
Source datasetuspto-grants-1995_06
ORD IDord-d091d214c9ce402593a44138f06172f3
Source noteuspto-grants-1995_06