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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093292Generated: November 3, 2026

N,N-Dimethylaniline → 4-Chloro-6-(trifluoromethyl)pyrimidin-2-amine

https://huagongshe.com/reaction/2093292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178508973HCID 178508973—
Product4-Chloro-6-(trifluoromethyl)pyrimidin-2-amineHCID 1308690722%

Reaction Steps

33.4 g (0.186 mol) of 4-hydroxy-6-trifluoromethylpyrimidin-2-ylamine are added in portions (in each case ca. 5 g) to a mixture of 85 ml of phosphorus oxychloride and 47.5 ml of dimethylaniline and the mixture is heated at reflux until the added solid has dissolved. The mixture is then heated at reflux for a further 90 minutes. After cooling, the reaction mixture is added to ice water while observing the safety precautions for phosphorus oxychloride. The aqueous phase is extracted with methylene chloride, the organic phase is separated off and dried with sodium sulfate, and the drying agent is filtered off. Following concentration by evaporation, 47.8 g of a crude mixture are obtained. Following column chromatographic separation with ethyl acetate/heptane as eluent, 8.5 g of 4-chloro-6-trifluoromethylpyrimidin-2-ylamine were obtained (solid, 22% yield, purity 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445408B2
Source datasetuspto-grants-2013_05
ORD IDord-7ffe31f7c4734dbeb3d84deccfa01aec
Source noteuspto-grants-2013_05