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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2355309생성일: 2026년 10월 25일

Tert-butyl 3-benzoylpiperidine-1-carboxylate → tert-Butyl 3-((R)-1-hydroxy-1-phenylhex-5-enyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2355309

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butyl 3-benzoylpiperidine-1-carboxylateHCID 57449677—
반응물HCID 178445862HCID 178445862—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 3-((R)-1-hydroxy-1-phenylhex-5-enyl)piperidine-1-carboxylateHCID 6719339088%

반응 조건

온도-78 °C

반응 단계

A stirred solution of tert-butyl 3-benzoylpiperidine-1-carboxylate (160 mg, 0.55 mmol) in dry THF (2 mL) was cooled to −70° C. and 4-pentenylmagnesium bromide in THF (1.8 mL of ˜2.5 M, 2.8 mmol) was added dropwise. The mixture was stirred at −78° C. and allowed to warm to rt overnight. The reaction was quenched with satd aq ammonium chloride. The aqueous layer was extracted with Et2O (3×). The combined organic layers were washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The crude material was purified by flash chromatography on a prepacked silica cartridge eluted with an EtOAc/hexanes gradient. tert-Butyl 3-((R)-1-hydroxy-1-phenylhex-5-enyl)piperidine-1-carboxylate (174 mg, 88%) was isolated as an oil. MS ESI+ve m/z 382 (M+Na)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07754737B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-0b496da3c9cb494fbab6dc9504565be3
출처 메모uspto-grants-2010_07