反応式
O1C2C(=CC=CC=2)C=CC1=O.[C:12](O)(=[O:29])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]>>[CH:12](=[O:29])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]参加物
3
実験手順
After the reaction, the autoclave was cooled with ice, and the pressure was reduced; subsequently, the reaction mixture was analyzed by FT-NMR using coumarin as an internal standard. The results confirmed that heptadecanoic acid was obtained in a yield of 78%, and heptadecanal was obtained in a yield of 21%.
後処理
- customAfter the reaction
- temperaturethe autoclave was cooled with ice
- customwas obtained in a yield of 78%
出典と根拠
- ORDレコード
- ord-99f5706563e94938a082bb3edd44fd6d
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08716501B2
関連ノート
読み込み中…