반응식
[CH2:1]([Li])[CH2:2][CH2:3][CH3:4].[I:6]I.C[Si](C)(C)[N-][Si](C)(C)C.[Na+].[CH2:18]([Si:20]([CH2:38][CH3:39])([CH2:36][CH3:37])[O:21][C@@H:22]([C:26]1[CH:27]=[C:28]2[C:33](=[CH:34][CH:35]=1)[N:32]=[CH:31][CH:30]=[CH:29]2)CC=O)[CH3:19]>[I-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)C.O1CCCC1.CCOCC>[I:6][C:3](=[CH:2][CH2:1][C@H:22]([C:26]1[CH:27]=[C:28]2[C:33](=[CH:34][CH:35]=1)[N:32]=[CH:31][CH:30]=[CH:29]2)[O:21][Si:20]([CH2:38][CH3:39])([CH2:36][CH3:37])[CH2:18][CH3:19])[CH3:4]참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
A suspension of ethyltriphenylphosphonium iodide (7.9 gm) in 150 mL of tetrahydrofuran is treated with a 2.5 M solution of n-butyllithium (7.17 mL) at ambient temperature. The resulting red solution is transferred via cannula into a vigorously stirred solution of iodine (4.54 gm) in 150 mL of tetrahydrofuran cooled to −78° C. The resulting suspension is stirred for 5 minutes, then gradually warmed to −30° C. A 1.0 M solution of sodium hexamethyldisilazide (17.3 mL) is then added dropwise to form a red solution. A solution of (3R)-3-(triethylsilyloxy)-3-(6-quinolyl)propanal (1.9 gm) in 10 mL of tetrahydrofuran is then added dropwise, and stirring is continued at −30° C. for 30 minutes. The mixture is diluted with ether, filtered through a pad of Celite, and concentrated. The product is purified by flash chromatography on silica gel.
후처리
- temperaturegradually warmed to −30° C
- customto form a red solution
- stirringstirring
- waitis continued at −30° C. for 30 minutes
- filtrationfiltered through a pad of Celite
- concentrationconcentrated
- customThe product is purified by flash chromatography on silica gel
출처 및 근거
- ORD 기록
- ord-fb07d3d7e0b74beeaa477216b98be3b2
- 출처 데이터셋
- uspto-grants-2007_02
- 특허 번호
- US07176235B2
연결된 노트
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