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HRID 443278作成日:2026年10月27日

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

https://huagongshe.com/reaction/443278

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic anhydrideHCID 9845—
反応物2,4-Dimethylpyridine 1-oxideHCID 70733—
溶媒DichloromethaneHCID 6344—
生成物(4-Methylpyridin-2-yl)methanolHCID 12325388—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05891889
出典データセットuspto-grants-1999_04
ORD IDord-dc555756eb054cb6a19efc7c9065d6bc
出典メモuspto-grants-1999_04