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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181437Generated: November 3, 2026

Triethylamine → 5-Azidomethyl-2-(trifluoromethyl)pyrimidine

https://huagongshe.com/reaction/1181437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
Reactant(2-(Trifluoromethyl)pyrimidin-5-yl)methanolHCID 24903629—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Azidomethyl-2-(trifluoromethyl)pyrimidineHCID 85869855100%

Reaction Steps

To a solution of 5-(hydroxymethyl)-2-(trifluoromethyl)pyrimidine (Description 119; 580 mg, 3.26 mmol) and triethylamine (0.55 ml, 3.91 mmol) in anhydrous dichioromethane (15 ml) cooled in an ice-bath was added dropwise methanesulfonyl chloride (0.28 ml, 3.59 mmol), and the resulting mixture stirred at room temperature for 1 hour. The mixture was washed with water and sat NaCl, dried over Na2SO4, filtered and evaporated. The residue was dissolved in anhydrous N,N-dimethylformamide (15 ml), sodium azide (233 mg, 3.59 mmol) was added and the resulting mixture stirred at room temperature overnight. The mixture was poured into water (100 ml) and extracted with EtOAc (3×15 ml). The combined EtOAc layers were washed with water (2×50 ml), saturated NaCl (25 ml), dried over Na2SO4, filtered and evaporated to give the title compound (660 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285563B2
Source datasetuspto-grants-2007_10
ORD IDord-2cb552c1a9ed462a9b417de6fe8e1ad1
Source noteuspto-grants-2007_10