Water → 5-Bromo-2-methyl-1-benzofuran

HRID 1699833ノート

反応式

HRID 1699833 の反応式
[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

5

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

  1. additionAfter the dropwise addition
  2. temperaturethe mixture was heated to room temperature
  3. temperaturecooled
  4. filtrationThe insoluble matter was filtered off
  5. customthe filtrate was partitioned
  6. extractionThe aqueous layer was extracted with methylene chloride
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationThe desiccant was filtered off
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. 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

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