戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 349740作成日:2026年10月25日

Acetic Acid → tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylate

https://huagongshe.com/reaction/349740

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Piperidin-4-olHCID 79341—
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—

反応手順

To 1-tert-butoxycarbonyl-4-piperidone (200 g, 1.01 mol) in tetrahydrofuran (THF) (1500 ml) was added 4-hydroxypiperidine (78.1 g, 0.77 mol). The resultant slurry was stirred for 30 minutes before cooling the reaction mixture with ice/water, acetic acid (47 ml) is then added (exotherm) which caused precipitation. The slurry was allowed to warm to room temperature before the addition of sodium triacetoxyborohydride (236 g, 1.12 mol) which was washed in with THF (500 ml). The resultant slurry was stirred overnight at room temperature. To the reaction mixture was added water (2000 ml) to give a solution. The solution was then extracted with diethyl ether (3×1800 ml). The aqueous phase was basified with 10% aq NaOH (950 ml) and extracted with dichloromethane (DCM) (3×1500 ml). The combined DCM layers are dried (MgSO4), filtered and the solvent removed to give the sub-titled compound as a yellow viscous oil, (177 g, 81%; MS: (M+H) 285).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179922B2
出典データセットuspto-grants-2007_02
ORD IDord-2f4469d729324b78879b0ef0abbd075b
出典メモuspto-grants-2007_02