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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tert-butyl 3-benzoylpiperidine-1-carboxylate | HCID 57449677 | — |
| 반응물 | HCID 178445862 | HCID 178445862 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 3-((R)-1-hydroxy-1-phenylhex-5-enyl)piperidine-1-carboxylate | HCID 67193390 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07754737B2 |
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| 출처 데이터셋 | uspto-grants-2010_07 |
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| ORD ID | ord-0b496da3c9cb494fbab6dc9504565be3 |
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| 출처 메모 | uspto-grants-2010_07 |
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