돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487369생성일: 2026년 10월 25일

Imidazole → (-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate

https://huagongshe.com/reaction/487369

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물rel-(1R,2S)-2-PhenylcyclohexanolHCID 102793—
반응물Triisopropylsilyl chlorideHCID 139400—
반응물Benzyloxyacetyl chlorideHCID 177085—
용매DimethylformamideHCID 6228—
용매PentaneHCID 8003—
생성물(-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetateHCID 1005992195%

반응 단계

To obtain 1c(-), a solution of (-)-(1R,2S)-2-phenyl-1-cyclohexyl hydroxyacetate (851 mg, 3.63 mmol) was prepared through esterification of benzyloxyacetyl chloride with (-)-(1R,2S)-2-phenyl-1-cyclohexanol followed by hydrogenolysis. Then, triisopropylsilyl chloride (840 mg, 4.36 mmol) and imidazole (618 mg, 9.08 mmol) in dimethylformamide (DMF) (1.7 mL) was stirred at room temperature for 12-20 hours. The mixture was poured into pentane (25 mL), and washed with water and brine. The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo. The crude product was subjected to a purification on a short silica gel column using hexane/chloroform (3/1) as the eluant to give pure 1c(-) (1.35 g, 95% yield) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294737
출처 데이터셋uspto-grants-1994_03
ORD IDord-8c8b239c359f4197a5536012d4027c08
출처 메모uspto-grants-1994_03