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]([CH2:37][CH3:38])([CH2:35][CH3:36])[O:21][C@@H:22]([C:26]([CH3:34])=[CH:27][C:28]1[N:29]=[C:30]([CH3:33])[S:31][CH:32]=1)CC=O)[CH3:19]>[I-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)C.C1COCC1.CCCCC>[I:6][C:3](=[CH:2][CH2:1][C@@H:22]([O:21][Si:20]([CH2:37][CH3:38])([CH2:35][CH3:36])[CH2:18][CH3:19])[C:26]([CH3:34])=[CH:27][C:28]1[N:29]=[C:30]([CH3:33])[S:31][CH:32]=1)[CH3:4]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- -30 °C
실험 절차
To a suspension of ethyltriphenylphosphonium iodide (7.90 g), in THF (150 mL) is added n-butyllithium (7.17 mL, 2.5 M in hexane) at ambient temperature. After disappearance of the solid material, the red solution is cannulated into a vigorously stirred solution of iodine (4.54 g) in THF (150 mL) at −78° C. The resulting dark brown suspension is stirred for 5 minutes and allowed to warm gradually to −30° C. A solution of sodium hexamethyldisilazide (17.3 mL, 1.0 M in THF) is added dropwise to afford a dark red solution. A solution of (3R)-3-(triethylsilyloxy)-4-methyl-5-(2-methylthiazol-4-yl)-pent-4-enal (2.0 g) in THF (10 mL) is slowly added, and stirring is continued at −30° C. for 30 minutes. The reaction mixture is diluted with pentane (100 mL), filtered through a pad of Celite, and concentrated. Purification by flash column chromatography on SiO2 (hexane/ethyl acetate, 15:1) affords the vinyl iodide.
후처리
- customto afford a dark red solution
- stirringstirring
- waitis continued at −30° C. for 30 minutes
- filtrationfiltered through a pad of Celite
- concentrationconcentrated
- customPurification by flash column chromatography on SiO2 (hexane/ethyl acetate, 15:1)
출처 및 근거
- ORD 기록
- ord-6924a6a04acf4f26b4eaf22e57c69ab9
- 출처 데이터셋
- uspto-grants-2007_02
- 특허 번호
- US07176235B2
연결된 노트
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