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HRID 33521作成日:2026年10月24日

Sodium borohydride → (5-(4-(Trifluoromethyl)phenyl)pyridin-3-yl)methanol

https://huagongshe.com/ja/reaction/33521

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物Methyl 5-(4-(trifluoromethyl)phenyl)nicotinateHCID 20099855—
溶媒EthanolHCID 702—
生成物(5-(4-(Trifluoromethyl)phenyl)pyridin-3-yl)methanolHCID 151948665.8%

反応条件

温度50 °C

反応手順

A solution of 335 mg (1.17 mmol) 5-(4-Trifluoromethyl-phenyl)-nicotinic acid methyl ester in 10.0 ml ethanol was treated at room temperature (r. t.) with 44 mg (1.17 mmol) of sodium borohydride. The mixture stirred two days at 50° C. Then it was poured on ice and extracted tree times with ethyl acetate. The combined organic phases were washed with water, dried (sodium sulphate) and evaporated. Chromatography on silica (eluent: ethyl acetate/methanol 5:1) gave 195 mg (64%) of [5-(4-Trifluoromethyl-phenyl)-pyridin-3-yl]-methanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429605B2
出典データセットuspto-grants-2008_09
ORD IDord-e9070980bb7a4af4980a657c08557dec
出典メモuspto-grants-2008_09