反応式
[CH3:1][O:2][CH:3]([O:6]C)[CH:4]=[CH2:5].[CH3:8]C1C=CC(S(O)(=O)=O)=CC=1.O.CCN([CH2:25][CH3:26])CC>CN(C=O)C.O>[CH3:8][CH2:1][O:2][CH:3]([O:6][CH2:25][CH3:26])[CH:4]=[CH2:5]参加物
6
実験手順
A solution of diol (Molecule 2.1) (1.5 g, 7.8 mmol) in 7.5 ml of dry DMF was treated with acrolein dimethyl acetal (4.62 ml, 39 mmol) and PTSA.H2O (0.371 g, 1.95 mmol). After stirring for 24 h at room temperature the reaction was stopped by addition of 1 ml of Et3N and poured out in 200 ml of H2O. The aqueous phase was extracted with toluene (3×100 ml) and the combined organics were washed once with brine (100 ml) and dried over MgSO4. Column chromatography of the residue over silica gel (cyclohexane/ethyl acetate: 85/15) afforded Molecule 2.2 (FIG. 4) as white crystals (1.306 g, 5.67 mmol, 73%).
後処理
- extractionThe aqueous phase was extracted with toluene (3×100 ml)
- washthe combined organics were washed once with brine (100 ml)
- dry with materialdried over MgSO4
出典と根拠
- ORDレコード
- ord-cc18b665322d4ac88e0828688dee6840
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07534871B2
関連ノート
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