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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245138생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/245138

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Piperidin-4-olHCID 79341—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매DichloromethaneHCID 6344—
생성물tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 983550839.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658636B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-132a556132594849b5222303bbdd35e9
출처 메모uspto-grants-2014_02