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HRID 23958作成日:2026年10月25日

1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/23958

反応式

関与物質

役割名称HCID仕込み量
反応物1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
反応物Borane;tetrahydrofuranHCID 2723981—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 276408185%

反応条件

温度0 °C

反応手順

1-Boc-isonipecotic acid (10.0 g, 214 mmol) was dissolved in THF (400 mL) and cooled to 0° C. A solution of BH3-THF (180 mL, 1 N in THF, 180 mmol) was added slowly. The mixture stirred for 1 h at 0° C. and was allowed to warm to room temperature for 12 h. The mixture was carefully quenched with water and diluted with ethyl acetate. The water layer was extracted with ethyl acetate. The organic layers were combined, washed with brine, dried (Na2SO4), filtered and concentrated to provide l-Boc-piperidine-4-methanol (7.98 g, 85%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855715B1
出典データセットuspto-grants-2005_02
ORD IDord-69907c3ae526490195aad8c034f65fdb
出典メモuspto-grants-2005_02