4-Benzyloxy-5-(4-fluorophenoxy)-1-pentanol → 4(S)-Acetyloxynonanal
反応式
C(OC(COC1C=CC(F)=CC=1)CCCO)C1C=CC=CC=1.[C:23]([O:26][C@@H:27]([CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])[CH2:28][CH2:29][CH2:30][OH:31])(=[O:25])[CH3:24]>>[C:23]([O:26][C@@H:27]([CH2:32][CH2:33][CH2:34][CH2:35][CH3:36])[CH2:28][CH2:29][CH:30]=[O:31])(=[O:25])[CH3:24]参加物
3
実験手順
This compound is prepared essentially by the method as described in Example 5, Step B-6, except that the 4-benzyloxy-5-(4-fluorophenoxy)pentanol is replaced by 4(S)acetyloxy-1-nonanol. This method provides the title compound as an essentially colorless oil.
後処理
- customThis compound is prepared essentially by the method
出典と根拠
- ORDレコード
- ord-efddd44528a44f72abd052717d43ad44
- 出典データセット
- uspto-grants-1978_07
- 特許番号
- US04102888
反応ノート
読み込み中…