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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401216Generated: November 1, 2026

(Diethylamino)sulfur trifluoride → 4-Chloro-6-(fluoromethyl)-5-methylpyrimidine

https://huagongshe.com/reaction/2401216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
Reactant(6-Chloro-5-methylpyrimidin-4-yl)methanolHCID 86762586—
SolventDichloromethaneHCID 6344—
Product4-Chloro-6-(fluoromethyl)-5-methylpyrimidineHCID 8667337874.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

DAST (1.5 mL, 11.35 mmol) was added to dichloromethane (DCM) (64 mL), cooled to −78° C. and treated dropwise with a solution of (6-chloro-5-methyl-4-pyrimidinyl)methanol (Intermediate 50, 1.70 g, 10.72 mmol) in DCM (24 mL) under argon. The resulting mixture was allowed to warm to room temperature and stirred for 3 hours. The reaction was quenched by adding water (45 ml) and extracted with DCM (×2). The DCM layers were separated, combined, dried under magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography (SP4, 40+M) eluting with a gradient of 0-50% ethyl acetate and iso-hexane. Product containing fractions were combined and evaporated under reduced pressure to give the title compound as a yellow oil (1.29 g) m/z (ES+) 161 (M+1), title compound is 42% pure by LCMS. Also contains 4-bromo-6-(fluoromethyl)-5-methylpyrimidine, m/z (ES+) 205, 207 (M+1) (44% by LCMS)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796283B2
Source datasetuspto-grants-2014_08
ORD IDord-0ac1a5344e2f4ebe9549d288aed52367
Source noteuspto-grants-2014_08