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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271456Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/271456

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktThionyl ChlorideHCID 24386—
Edukt(2-Methyl-6-(trifluoromethyl)pyridin-3-yl)methanolHCID 2760122—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Chloromethyl)-2-methyl-6-(trifluoromethyl)pyridineHCID 5983481592,1%

Reaktionsschritte

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 saturated aqueous NaCl (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]30 =210.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452892B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-33eaa5365fb94577a865ba2c68932c80
Quellennotizuspto-grants-2008_11