Sodium Hydroxide → Sodium tridecanoate
反応式
[C:1]([O:15]C)(=[O:14])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[OH-].[Na+:18]>O>[C:1]([O-:15])(=[O:14])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[Na+:18]参加物
実験手順
A mixture of methyl tridecanoate isomers, 95% pure and containing 65% methyl n-tridecanoate, was subjected to partial hydrolysis under basic conditions. A 10 ml amount of the isomer mixture was placed with 10 ml water in a flask equipped with a reflux condenser, along with 0.15 gram sodium hydroxide. The mixture was heated to reflux with stirring. After forty minutes, a sample was taken from the organic phase and a sodium tridecanoate white crystalline solid formed therein upon cooling. The sample was acidified with sulfuric acid and solids were separated by filtration and washed three times with water. By gas chromatographic analysis it was determined that the material was 64.9% hydrolyzed, and that 97.5% of the tridecanoic acid was n-tridecanoic acids, representing a substantial enrichment from the original 65%.
後処理
- customwas subjected to partial hydrolysis under basic conditions
- temperatureThe mixture was heated
- temperatureto reflux
- waitAfter forty minutes
出典と根拠
- ORDレコード
- ord-0788386cb1034439b95380788a6d9698
- 出典データセット
- uspto-grants-1980_07
- 特許番号
- US04215065
反応ノート
読み込み中…