反応式
[CH:1](Cl)([OH:5])[CH:2]([Cl:4])[Cl:3].C(N([CH2:12][CH3:13])CC)C.C([Cl:18])(=O)C=C.O.C([O:22][CH2:23]C)C>>[Cl:3][C:2]([Cl:18])([Cl:4])[CH2:1][O:5][C:23](=[O:22])[CH:12]=[CH2:13]参加物
6
実験手順
A first solution including trichloroethanol (30 g, 201 mmol) and triethylamine (22.36 g, 221 mmol) dissolved in 50 g of diethylether was prepared. A second solution comprising acryloyl chloride (20 g, 221 mmol) dissolved in 50 g of diethylether was added dropwise to the first solution followed by stirring for four hours at room temperature. The resulting solution was then added to water, and the organic phase was extracted. The organic phase was distilled to yield 32.28 g of TCEA (78.9% yield).
後処理
- customwas prepared
- additionwas added dropwise to the first solution
- extractionthe organic phase was extracted
- distillationThe organic phase was distilled
出典と根拠
- ORDレコード
- ord-d55e2980bf924dceb7cf6043b103ac70
- 出典データセット
- uspto-grants-2002_12
- 特許番号
- US06495305B1
関連ノート
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