反応式
[OH:1][CH:2]1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH:13]=[CH:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]CC[C:3]1=[O:22].OC1CCCCCCC=CCCCCCCCCC1=O>>[OH:1][CH:2]1[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][C:3]1=[O:22]参加物
3
実験手順
2-Hydroxy-11-cycloeicosenone of Synthesis Example 7 was replaced by 2-hydroxy-9-cyclooctadecenone (1.0 g, 3.54 mmol), and a hydrogenation and subsequent treatment were performed under the same conditions as in Synthesis Example 7, to yield 1.0 g of 2-hydroxycyclooctadecanone (quantitative yield).
後処理
- customa hydrogenation and subsequent treatment were performed under the same conditions as in Synthesis Example 7
出典と根拠
- ORDレコード
- ord-b77a471df5e74655ac77e43502bce19d
- 出典データセット
- uspto-grants-2004_07
- 特許番号
- US06759557B2
関連ノート
読み込み中…