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HRID 2202230作成日:2026年10月27日

Formaldehyde → 2-(6-Methoxypyridin-2-yl)ethan-1-ol

https://huagongshe.com/reaction/2202230

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sodium ChlorideHCID 5234—
反応物2-Methoxy-6-methylpyridineHCID 5324773—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
生成物2-(6-Methoxypyridin-2-yl)ethan-1-olHCID 1531987137%

反応条件

温度-78 °C

反応手順

1.6M n-Butyllithium/hexane solution (282 mL, 451.96 mmol) was added dropwise to a solution of 2-methoxy-6-methylpyridine (50.60 g, 410.87 mmol) in THF (625 mL) over 1 hr at −78° C. under argon atmosphere. The reaction mixture was stirred at −78° C. for 45 min, paraformaldehyde (49.3 g, 1643.49 mmol) was added thereto at −78° C., and the mixture was stirred vigorously at room temperature for 3.5 hr. The reaction mixture was poured into ice water (1000 mL), and NaCl was added thereto to give a saturated solution. The saturated solution was extracted with a mixed solvent of ethyl acetate/THF (3:1) (×3). The organic layer was washed with water and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 8→50% ethyl acetate/hexane) to give 2-(6-methoxypyridin-2-yl)ethanol (23.22 g, 152 mmol, 37%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09365520B2
出典データセットuspto-grants-2016_06
ORD IDord-4f377e6bfab64d51a68200e2dbd8c104
出典メモuspto-grants-2016_06