反応式
C([O:4][C:5](O)([OH:8])CC)C=C.N1[CH:15]=[CH:14][CH:13]=CC=1.CN([C:19]1[CH:24]=[CH:23]C=CN=1)C.[C:25]([O:30][C:31](=[O:35])[C:32]([CH3:34])=[CH2:33])(=[O:29])[C:26]([CH3:28])=C>C(Cl)(Cl)Cl>[C:31]([O:30][C:25]([O:29][CH2:15][CH:14]=[CH2:13])([O:8][C:5](=[O:4])[C:24]([CH3:23])=[CH2:19])[CH2:26][CH3:28])(=[O:35])[C:32]([CH3:34])=[CH2:33]参加物
6
反応条件
- 温度
- 50 °C
実験手順
Allyloxypropanediol (0.5 equivalents) was stirred in chloroform with pyridine (1 equivalent) and dimethlaminopyridine (0.05 equivalent) and warmed to 50° C. Methacrylic anhydride was added dropwise and stirring was continued until starting diol was no longer detected by gas chromatography. The reaction mixture was then washed with dilute hydrochloric acid, sodium bicarbonate and water. Concentration on a rotary evaporator gave the crude product.
後処理
- washThe reaction mixture was then washed with dilute hydrochloric acid, sodium bicarbonate and water
- concentrationConcentration
- customon a rotary evaporator
出典と根拠
- ORDレコード
- ord-bdfe362f90b5432f81952ef2a1d2d655
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04640940
関連ノート
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