Aluminum(III) Chloride → 1-(2-Bromo-5-hydroxy-4-methoxyphenyl)ethan-1-one

HRID 41942ノート

反応式

HRID 41942 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([O:10]C(C)C)=[CH:4][C:3]=1[C:14](=[O:16])[CH3:15].[Al+3].[Cl-].[Cl-].[Cl-]>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([OH:10])=[CH:4][C:3]=1[C:14](=[O:16])[CH3:15]

参加物

4

反応条件

温度
18 °C

実験手順

A solution of ketone 38 (220 mg, 0.766 mmol) in dry CH2Cl2 (2.0 mL) was treated with AlCl3 (306 mg, 2.29 mmol) and the resulting mixture stirred at 18° C. under a nitrogen atmosphere for 2 h. The ensuing mixture was partitioned between H2O (5 mL) and CH2Cl2 (5 mL) then the separated aqueous phase extracted with CH2Cl2 (1×15 mL). The combined organic fractions were dried (MgSO4), filtered and concentrated under reduced pressure and the ensuing residue subjected to flash chromatography (15:85 v/v ethyl acetate/hexane elution) to afford the title compound 39 (184 mg, 98%) as a pale-yellow solid, m.p. 109.7-111.4° C., Rf 0.4 in 1:1 v/v ethyl acetate/hexane.

後処理

  1. customThe ensuing mixture was partitioned between H2O (5 mL) and CH2Cl2 (5 mL)
  2. extractionthe separated aqueous phase extracted with CH2Cl2 (1×15 mL)
  3. dry with materialThe combined organic fractions were dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. washthe ensuing residue subjected to flash chromatography (15:85 v/v ethyl acetate/hexane elution)

出典と根拠

ORDレコード
ord-cd01f9518abd4690b32111d9710e19ff
出典データセット
uspto-grants-2013_09
特許番号
US08536157B2

反応ノート

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