Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443278Generated: October 25, 2026

Trifluoroacetic anhydride → (4-Methylpyridin-2-yl)methanol

https://huagongshe.com/reaction/443278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2,4-Dimethylpyridine 1-oxideHCID 70733—
SolventDichloromethaneHCID 6344—
Product(4-Methylpyridin-2-yl)methanolHCID 12325388—

Reaction Steps

A mixture of 2,4-dimethylpyridine N-oxide (10.9 g, 88.5 mmol) and trifluoroacetic anhydride (31 mL, 219 mmol) in dichloromethane (75 mL) was stirred at room temp. overnight. The product mixture was concentrated under vacuum. The residue was dissolved in a mixture of dichloromethane (75 mL) and aqueous sodium carbonate (225 mL, 2M), and stirred vigorously for 4 h. The resultant mixture was diluted with dichloromethane. The organic extract was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was subjected to column chromatography on silica gel eluting with 1-2% methanol in chloroform gradient. Collection and concentration of appropriate fractions provided 2-hydroxymethyl-4-methylpyridine as clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-dc555756eb054cb6a19efc7c9065d6bc
Source noteuspto-grants-1999_04