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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101399Generated: November 2, 2026

Dimethylformamide → 3-(Chloromethyl)-2-methyl-6-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/2101399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant(2-Methyl-6-(trifluoromethyl)pyridin-3-yl)methanolHCID 2760122—
SolventDichloromethaneHCID 6344—
Product3-(Chloromethyl)-2-methyl-6-(trifluoromethyl)pyridineHCID 5983481592.1%

Reaction Steps

To a solution of (2-methyl-6-(trifluoromethyl)pyridin-3-yl)methanol (14.5 g, 71 mmol) in 100 mL CH2Cl2 at room temperature under argon was added SOCl2 (16.8 g, 142 mmol), followed by about 1.5 mL DMF, which was added to re-dissolve the rapidly formed, precipitating hydrochloride salt of the starting material. The resulting reaction mixture was stirred for 16 h. HPLC/MS analysis indicated that the reaction was complete. Solvent was evaporated under vacuum. The resulting residue was dissolved in 200 mL Et2O, and the resulting solution was washed with 10% aqueous sodium carbonate solution (100 mL), then brine (100 mL). The organic phase was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under vacuum to obtain 13.7 g of the title compound as a tan oil, which was greater than 98% pure. HPLC/MS: retention time=2.9 min, [M+H]+=210.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572808B2
Source datasetuspto-grants-2009_08
ORD IDord-404b8adb83c048d7a2c58085bc514ecc
Source noteuspto-grants-2009_08