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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | (6-Chloro-5-methylpyrimidin-4-yl)methanol | HCID 86762586 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-6-(fluoromethyl)-5-methylpyrimidine | HCID 86673378 | 74.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796283B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-0ac1a5344e2f4ebe9549d288aed52367 |
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| Source note | uspto-grants-2014_08 |
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