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HRID 54547作成日:2026年10月24日

Water → 2-(1-(4-Fluorobenzyl)piperidin-4-yl)ethan-1-ol

https://huagongshe.com/ja/reaction/54547

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物p-Toluenesulfonic acidHCID 6101—
反応物4-FluorobenzaldehydeHCID 68023—
反応物4-PiperidineethanolHCID 73953—
溶媒BenzeneHCID 241—
生成物2-(1-(4-Fluorobenzyl)piperidin-4-yl)ethan-1-olHCID 10561862—

反応手順

A mixture of 4-(2-hydroxyethyl)piperidine (21.5 g), 4-fluorobenzaldehyde (17.5 ml) and p-toluene sulfonic acid (3 mg) in benzene (200 ml) was refluxed with separating water as the benzene azeotrope. After 2 hours, the mixture was evaporated in vacuo. The residue was dissolved in methanol (200 ml) and sodium borohydride (6.3 g) was added thereto at 5° C. After stirring at ambient temperature for 1 hour, the mixture was evaporated in vacuo. 4N Hydrochloric acid (200 ml) was added to the residue and washed with ethyl acetate. The aqueous layer was made basic to pH 10 with potassium carbonate and extracted with ethyl acetate. The extract was washed with water and brine, and dried over magnesium sulfate, and evaporated in vacuo to give 1-(4-fluorobenzyl)-4-(2-hydroxyethyl)piperidine (32.0 g) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622976
出典データセットuspto-grants-1997_04
ORD IDord-81c94a8cf3a54d16a3ac4f055b91e857
出典メモuspto-grants-1997_04