Water → 5-Bromo-2-methyl-1-benzofuran
反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:12]C)=[C:6]([CH2:8][C:9](=O)[CH3:10])[CH:7]=1.B(Br)(Br)Br.O>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[O:12][C:9]([CH3:10])=[CH:8][C:6]=2[CH:7]=1参加物
反応条件
- 温度
- -70 °C
実験手順
(5-Bromo-2-methoxyphenyl)acetone (6.6 g, 28.6 mmol) was dissolved in methylene chloride (50 ml) and cooled to −70° C. Thereto was dropwise added a 1 M solution (28.6 ml, 28.6 mmol) of boron tribromide in methylene chloride over 15 min. After the dropwise addition, the mixture was heated to room temperature and stirred for 1.5 hr. Then, the reaction mixture was ice-cooled and water (50 ml) was added. The insoluble matter was filtered off and the filtrate was partitioned. The aqueous layer was extracted with methylene chloride. The organic layers were combined, and dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=30/1) to give the objective compound (3.45 g, 57%) as a colorless liquid.
後処理
- additionAfter the dropwise addition
- temperaturethe mixture was heated to room temperature
- temperaturecooled
- filtrationThe insoluble matter was filtered off
- customthe filtrate was partitioned
- extractionThe aqueous layer was extracted with methylene chloride
- dry with materialdried over anhydrous sodium sulfate
- filtrationThe desiccant was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=30/1)
出典と根拠
- ORDレコード
- ord-cb9b91d856bc4908b7f8bdd0899f5291
- 出典データセット
- uspto-grants-2002_02
- 特許番号
- US06348474B1
反応ノート
読み込み中…