反応式
[CH:1]([C:4]1[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[CH:7]=[C:6]([CH:13]([CH3:15])[CH3:14])[C:5]=1[S:16](Cl)(=[O:18])=[O:17])([CH3:3])[CH3:2].[N-:20]=[N+:21]=[N-:22].[Na+]>CC(C)=O.C(O)C.O>[CH:1]([C:4]1[CH:9]=[C:8]([CH:10]([CH3:12])[CH3:11])[CH:7]=[C:6]([CH:13]([CH3:15])[CH3:14])[C:5]=1[S:16]([N:20]=[N+:21]=[N-:22])(=[O:18])=[O:17])([CH3:3])[CH3:2]参加物
実験手順
To a stirred solution of 2,4,6-triisopropylbenzenesulfonyl chloride (18.2 g, 60.0 mmol) in reagen acetone (70 mL) is added a solution of sodium azide (4.3 g, 60 μmol) in ethanol-H2O 1:1 (40 mL). The temperature of the mixture rises from 21° C. to 29° C. during the addition. After stirring at room temperature for 2 hours, the reaction mixture is partitioned between dichloromethane and half saturated brine. The aqueous solution is extracted with dichloromethane (3×), the combined organic solution is washed with half saturated brine, and dried (magnesium sulfate). Removal of solvent in vacuo gives a colorless oil which is purified by flash chromatography (silica gel, hexane ethyl acetate/4:1) to yield the title compound as a white solid, 18.5 g; mp 44°-44.5° C. (Evans, D., et al, Journal of the American Chemical Society 112:4011 (1990); mp 43°-44° C.).
後処理
- additionThe temperature of the mixture rises from 21° C. to 29° C. during the addition
- customthe reaction mixture is partitioned between dichloromethane and half saturated brine
- extractionThe aqueous solution is extracted with dichloromethane (3×)
- washthe combined organic solution is washed with half saturated brine
- dry with materialdried (magnesium sulfate)
- customRemoval of solvent in vacuo
- customgives a colorless oil which
- customis purified by flash chromatography (silica gel, hexane ethyl acetate/4:1)
出典と根拠
- ORDレコード
- ord-ff384bb99eee4cb7a1683daa94ac6316
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05264577
関連ノート
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