반응식
[Si]([O:8][C:9]1[C:14]([CH2:15][CH2:16][CH3:17])=[CH:13][C:12]([CH:18]=[CH2:19])=[CH:11][C:10]=1[CH2:20][CH2:21][CH3:22])(C(C)(C)C)(C)C.[F-].C([N+](CCCC)(CCCC)CCCC)CCC.CCOCC.C(OCC)(=O)C>C1COCC1>[CH2:15]([C:14]1[CH:13]=[C:12]([CH:18]=[CH2:19])[CH:11]=[C:10]([CH2:20][CH2:21][CH3:22])[C:9]=1[OH:8])[CH2:16][CH3:17]참가 물질
5
실험 절차
The title compound was prepared from t-butyldimethyl-silyloxy-2,6-dipropyl-4-vinylbenzene (Step B, Example 14) by treatment with tetrabutylammonium fluoride in THF for a few hours. It was poured into ether/ethyl acetate mixture and washed with brine. After removal of the solvent the crude product was purified by flash column chromatography using ethyl acetate/hexane as eluent.
후처리
- washwashed with brine
- customAfter removal of the solvent the crude product
- customwas purified by flash column chromatography
출처 및 근거
- ORD 기록
- ord-58545c78ce21451da326644a9ef52454
- 출처 데이터셋
- uspto-grants-1998_06
- 특허 번호
- US05767310
연결된 노트
불러오는 중…