反応式
CCCC(O[CH2:8][C:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:10])CC.[CH3:17][C:18]1[CH:19]=[C:20]([CH:23]=[C:24]([CH3:27])[C:25]=1[OH:26])[CH:21]=O>>[CH2:9]([O:10][C:14]1[CH:13]=[CH:12][C:11]([C:9](=[O:10])[CH:8]=[CH:21][C:20]2[CH:19]=[C:18]([CH3:17])[C:25]([OH:26])=[C:24]([CH3:27])[CH:23]=2)=[CH:16][CH:15]=1)[CH2:11][CH2:12][CH2:13][CH2:14][CH3:15]参加物
3
実験手順
This compound was synthesized from 4-hexyloxyacetophenone and 3,5-dimethyl-4-hydroxybenzaldehyde according to general method 1 described hereinabove. The product crystallized at the end of the reaction and was dried. Yield: 63%
後処理
- customThe product crystallized at the end of the reaction
- customwas dried
出典と根拠
- ORDレコード
- ord-8a666137ddbb47e6b229b3ccd4636024
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07385082B2
関連ノート
読み込み中…