反応式
[C:1]1([CH2:7][C:8]#[N:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:10]([O:15][CH2:16][CH3:17])(=[O:14])[C:11]([O-])=[O:12].[O-]CC.[Na+].[Na]>C(O)C>[C:8]([CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[C:11](=[O:12])[C:10]([O:15][CH2:16][CH3:17])=[O:14])#[N:9]参加物
6
実験手順
A mixture of 117.1 g. (1.0 mol.) of phenylacetonitrile and 326 ml. (2.4 mol.) of ethyl oxalate was added to an ethanol solution of sodium ethoxide [prepared by dissolving 23.8 g. (1.08 g.-atom) of sodium in 500 ml. of absolute ethanol] and refluxed two hours. After cooling, diluting with 2500 ml. of water and extracting with ether, the solution was acidified with acetic acid. The solid was removed and washed with water to give ethyl 3-cyano-3-phenylpyruvate, m.p. 127°-129°.
後処理
- additionA mixture of 117.1 g
- temperaturerefluxed two hours
- temperatureAfter cooling
- additiondiluting with 2500 ml
- extractionof water and extracting with ether
- customThe solid was removed
- washwashed with water
出典と根拠
- ORDレコード
- ord-7178fb7bbb534adcad6de89e9b15b2a8
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03947580
関連ノート
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