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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1604835생성일: 2026년 10월 25일

TMS-Imidazole → (4aR,5R,8aR)-5-[(3E,5E)-(R)-(1,7-dimethyl-7-trimethylsilanyloxy-octa-3,5-dienyl)]-4a-methyl-octahydro-naphthalen-1-one

https://huagongshe.com/reaction/1604835

반응식

참여 물질

역할이름HCID투입량
반응물TMS-ImidazoleHCID 14420972—
반응물(4aR,5R,8aR)-5-((3E,5E)-(R)-7-hydroxy-1,7-dimethyl-octa-3,5-dienyl)-4a-methyl-octahydro-naphthalen-1-oneHCID 86754888—
용매DichloromethaneHCID 6344—
생성물(4aR,5R,8aR)-5-[(3E,5E)-(R)-(1,7-dimethyl-7-trimethylsilanyloxy-octa-3,5-dienyl)]-4a-methyl-octahydro-naphthalen-1-oneHCID 86754887—

반응 단계

323 mg of (4aR,5R,8aR)-5-((3E,5E)-(R)-7-hydroxy-1,7-dimethyl-octa-3,5-dienyl)-4a-methyl-octahydro-naphthalen-1-one, was reacted at 40° with 1.33 ml of TMS-imidazole (9 equivalents) in 8 ml of CH2Cl2. After a few hours the mixture was poured onto crushed ice, extracted with ether, washed with water, dried over sodium sulfate and evaporated to dryness. Flash chromatography (SiO2, hexane/AcOEt=9/1) yielded 326 mg of (4aR,5R,8aR)-5-[(3E,5E)-(R)-(1,7-dimethyl-7-trimethylsilanyloxy-octa-3,5-dienyl)]-4a-methyl-octahydro-naphthalen-1-one as colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05994569
출처 데이터셋uspto-grants-1999_11
ORD IDord-a4756f5bf9f944ceb0f4c7886654674e
출처 메모uspto-grants-1999_11