4'-Acetamido-3'-bromoacetophenone → 1-(4-Amino-3-bromo-phenyl)-ethanone
反応式
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10]C(=O)C)=[C:6]([Br:14])[CH:5]=1)(=[O:3])[CH3:2]>Cl>[NH2:10][C:7]1[CH:8]=[CH:9][C:4]([C:1](=[O:3])[CH3:2])=[CH:5][C:6]=1[Br:14]参加物
3
実験手順
A solution of N-(4-Acetyl-2-bromo-phenyl)-acetamide (10.0 g, 39.05 mmol) in concentrated hydrochloric acid (200 mL) was stirred for 5 h under reflux. The reaction mixture was concentrated under reduced pressure. The residue was treated with a saturated aqueous solution of NaHCO3 (75 mL), extracted with CH2Cl2 (2×70 mL) and dried over Na2SO4. Evaporation leads to the product (8.35 g, 100%) which was used in step 2 without further purification.
後処理
- temperatureunder reflux
- concentrationThe reaction mixture was concentrated under reduced pressure
- additionThe residue was treated with a saturated aqueous solution of NaHCO3 (75 mL)
- extractionextracted with CH2Cl2 (2×70 mL)
- dry with materialdried over Na2SO4
- customEvaporation
- customwas used in step 2 without further purification
出典と根拠
- ORDレコード
- ord-b0138cc4b3474d00af8ea8ffcd007ca8
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08143242B2
反応ノート
読み込み中…