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HRID 245138作成日:2026年10月26日

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

https://huagongshe.com/reaction/245138

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DichloromethaneHCID 6344—
生成物tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 983550839.1%

反応手順

A mixture of 1,1-dimethylethyl 4-oxo-1-piperidinecarboxylate (3.15 g, 15.8 mmol), 4-piperidinol (1.0 g, 9.88 mmol), and acetic acid (0.8 mL) in methylene chloride (30 mL) was stirred for 3 h at room temperature. Sodium triacetoxyborohydride (3.35 g, 15.8 mmol) was added and the mixture was stirred at room temperature for 18 h. The solvent was removed under reduced pressure, and the residue was dissolved in methylene chloride and washed with 1N HCl. The aqueous phase was extracted with ether (3×10 mL) and adjusted to pH 9-10 with 1N NaOH. The basic aqueous mixture was extracted with methylene chloride (3×10 mL). The combined organic extracts were concentrated in vacuo to afford 1,1-dimethylethyl 4-hydroxy-1,4′-bipiperidine-1′-carboxylate (1.1 g, 39% yield). This material was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658636B2
出典データセットuspto-grants-2014_02
ORD IDord-132a556132594849b5222303bbdd35e9
出典メモuspto-grants-2014_02