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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23783생성일: 2026년 10월 23일

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol

https://huagongshe.com/ko/reaction/23783

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물Sodium BicarbonateHCID 516892—
반응물(S)-3-(t-butyldimethylsilyloxy)-5-(4-methoxy-benzyloxy)-1-phenyl pentaneHCID 69589755—
용매Water methylene chlorideHCID 21908982—
생성물(S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-olHCID 6958999399.4%

반응 단계

(S)-3-(t-butyl dimethylsilyloxy)-5-(4-methoxy-benzyloxy)-1-phenyl pentane (15 g, 36.2 mmol) was dissolved in a solvent mixture of dichloromethane-water (20:1) (252 ml). DDQ (8.2 g, 36.2 mmol) was added thereto and the mixture was stirred for 30 minutes at room temperature. After completion of the reaction, saturated aqueous NaHCO3 solution (100 ml) was added to the reaction solution to stop the reaction. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The organic layers were combined, washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution, dried over MgSO4, filtered, and concentrated. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to give (S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol (10.6 g, Yield 99%) of a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852880B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-1c47ced5a42f41fc94e54e9b138b5b44
출처 메모uspto-grants-2005_02