Acetyl chloride → HCID 66640898、化合物
反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:6]([CH:9]=1)[CH:7]=O.[Li+].C[Si]([N-:22][Si](C)(C)C)(C)C.[C:27](Cl)(=[O:29])[CH3:28].Cl[Si:32]([CH3:35])([CH3:34])[CH3:33]>C(N(CC)CC)C>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:6]([CH:7]=[N:22][C:27]([O:29][Si:32]([CH3:35])([CH3:34])[CH3:33])=[CH2:28])[CH:9]=1参加物
6
実験手順
In a manner similar to the method described in Example 112b, 5-fluoro-2-(cyclohexyloxy)-benzaldehyde was treated with LHMDS, acetyl chloride, triethylamine and chloro-trimethyl-silane to give the desired compound, which was directly used for the next step.
出典と根拠
- ORDレコード
- ord-3a2fb28f9b744945b145724373558611
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08134001B2
反応ノート
読み込み中…