反応式
[C:1]1(=[O:16])[CH2:15]CCCCCC[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.[C:17](OC(=O)C)(=O)C.C[C:25](=[O:33])[CH:26]=[CH:27]CCCCC.C(OC(=O)CC)(=O)CC>>[C:25]([O:16][C:1](=[CH:2][CH:3]([CH3:17])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH3:15])(=[O:33])[CH2:26][CH3:27]参加物
5
実験手順
The same procedure as described in Example 1 (a) was carried out, except that 2-cyclopentadecenone and acetic anhydride were replaced with 3-nonen-2-one and propionic anhydride, respectively, to produce 4-methyl-2-nonene-2-yl propionate in 83% yield. E/Z=13/87.
出典と根拠
- ORDレコード
- ord-78310bfcd33c4c6886ab0ae18d9ccfda
- 出典データセット
- uspto-grants-2010_12
- 特許番号
- US07846701B2
関連ノート
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