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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 655161생성일: 2026년 10월 25일

3-Iodopyridine → (1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-ol

https://huagongshe.com/reaction/655161

반응식

참여 물질

역할이름HCID투입량
반응물3-IodopyridineHCID 70714—
반응물rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 10154103—
반응물HCID 178418546HCID 178418546—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
용매Ammonium ChlorideHCID 25517—
생성물(1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-olHCID 5948612155.3%

반응 단계

To a solution of 3-Iodopyridine (13.0 g, 63.3 mmol) in THF (30 mL) was added i-PrMgCl (38.0 mL, 76.0 mmol) at 3-9° C. After stirring was continued at room temperature for 30 min, CuCN (567 mg, 6.33 mmol) was added to the solution at 2° C. After stirring was continued at 3° C. for 30 min, to the resulting solution were added (1R,4S)-4-hydroxycyclopent-2-enyl acetate (3.00 g, 21.1 mmol) in THF (30 mL). The whole mixture was stirred at the room temperature for 2 h, and diluted with saturated NH4Cl with vigorous stirring. The products were extracted with EtOAc three times, and the combined layers were dried over Na2SO4. After concentration under reduced pressure, the residue was purified by column chromatography (NH, Hexane/EtOAc=4/1) to yield (1S,4S)-4-(3-pyridyl)-2-cyclopenten-1-ol (1.88 g, 55%) as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08071591B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-d22fd8b1de6d415ca3aaf9eda8aed6b2
출처 메모uspto-grants-2011_12