Pyridine → Allyloxypropanediol Dimethacrylate

HRID 235679

反応式

HRID 235679 の反応式
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

  1. washThe reaction mixture was then washed with dilute hydrochloric acid, sodium bicarbonate and water
  2. concentrationConcentration
  3. 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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