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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1243207생성일: 2026년 10월 27일

Imidazole → 2-Cyclopenten-1-ol, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, cis-

https://huagongshe.com/reaction/1243207

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물4-Cyclopentene-1,3-diol, 1-acetate, (1R,3S)-rel-HCID 9855498—
용매TetrahydrofuranHCID 8028—
생성물2-Cyclopenten-1-ol, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, cis-HCID 10176747—

반응 단계

To a solution of (1R,4S)-4-acetoxy-2-cyclopenten-1-ol (1.0 g, 7.03 mmol) (Fluka) and imidazole (960 mg, 14.06 mmol) (Aldrich) in tetrahydrofuran (65 mL) at 0° C. was added tert-butyldimethylsilyl chloride (1.27 g, 8.44 mmol) (Aldrich). The mixture was allowed to warm slowly to room temperature, stirred overnight and then partitioned between ethyl acetate and water. The organic layer was collected, dried over sodium sulfate, filtered and concentrated to a residue that was dissolved in methanol (approximately 45 mL). To this solution was added potassium carbonate (1.17 g, 8.44 mmol) and the mixture stirred overnight. The reaction mixture was then partitioned between ethyl acetate and water. The organic layer was collected, dried over sodium sulfate, filtered and concentrated to a residue that was purified by silica gel column chromatography with a 0–30% diethyl ether in hexanes gradient to give (+)-(1S,4R)-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enol as a colorless oil. (Yield 1.43 g, 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07115740B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-38f084e084c84450ba3e7433212cac2d
출처 메모uspto-grants-2006_10