Acetyl chloride → HCID 58188103、化合物
反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:11][CH:12]2[CH2:16][CH2:15][CH2:14][CH2:13]2)[CH:10]=1)[C:5]([OH:7])=[O:6].[C:17](Cl)(=O)C>CO>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([S:11][CH:12]2[CH2:13][CH2:14][CH2:15][CH2:16]2)[CH:10]=1)[C:5]([O:7][CH3:17])=[O:6]参加物
4
実験手順
A solution of 3-bromo-5-(cyclopentylthio)benzoic acid (1.49 g, 4.95 mmol) in methanol (40 mL) was treated with acetyl chloride (3.87 mL, 54.4 mmol) at 0° C. The reaction mixture was heated to reflux overnight, and then concentrated under reduced pressure. The residue was purified by flash chromatography (0-20% EtOAc/hexane) to afford the title compound as a colorless oil.
後処理
- temperatureThe reaction mixture was heated
- temperatureto reflux overnight
- concentrationconcentrated under reduced pressure
- customThe residue was purified by flash chromatography (0-20% EtOAc/hexane)
出典と根拠
- ORDレコード
- ord-6041f20e2bb7498fadc36ca541e96e32
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08946439B2
反応ノート
読み込み中…