反応式
CCC(=O)CC(=O)CC.[CH3:10][CH:11]([C:13](=[O:20])[CH2:14][C:15](=[O:19])[CH:16]([CH3:18])[CH3:17])[CH3:12]>>[CH3:18][CH:16]([CH:15]([OH:19])[CH2:14][CH:13]([OH:20])[CH:11]([CH3:12])[CH3:10])[CH3:17]参加物
3
実験手順
Synthesis procedure was similar to that described in synthetic example 19(1), except that 3,5-heptandione was replaced by 2,6-dimethyl-3,5-heptandione, and finally the product was purified by distilling under reduced pressure. 2,6-dimethyl-3,5-heptandiol as a colorless liquid was obtained with a yield of 90%.
後処理
- customSynthesis procedure
- customfinally the product was purified
- distillationby distilling under reduced pressure
出典と根拠
- ORDレコード
- ord-04ac086d882341f888b8d3d82bf35919
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07388061B2
関連ノート
読み込み中…