Acetyl chloride → 1-(4-Bromo-5-chloro-2-hydroxyphenyl)ethanone

HRID 626832ノート

反応式

HRID 626832 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([O:8]C)[CH:5]=[CH:4][C:3]=1[Cl:10].[C:11](Cl)(=[O:13])[CH3:12].[Cl-].[Cl-].[Cl-].[Al+3]>C(=S)=S>[Br:1][C:2]1[C:3]([Cl:10])=[CH:4][C:5]([C:11](=[O:13])[CH3:12])=[C:6]([OH:8])[CH:7]=1

参加物

5

反応物 3

HCID 6367Acetyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 242120812-Bromo-1-chloro-4-methoxybenzene

生成物 1

HCID 595641771-(4-Bromo-5-chloro-2-hydroxyphenyl)ethanone収率 99.3%

試薬・触媒・溶媒 1

HCID 6348Carbon Disulfide溶媒

実験手順

The 2-bromo-1-chloro-4-methoxybenzene (25.0 g, 113 mmol) [Oakwood cat#035670] was dissolved in carbon disulfide (250 mL), and the acetyl chloride (12 mL, 170 mmol) and aluminum trichloride (37.6 g, 282 mmol) were added. The reaction was heated to reflux and monitored by LC/MS. After heating for 1 h, the reaction became two layers. The reaction allowed to cool to room temperature and poured over ice. The slurry was extracted with ethyl acetate 3×, the combined organic layer was washed with brine, dried over magnesium sulfate and concentrated to give 1-(4-bromo-5-chloro-2-hydroxyphenyl)ethanone as a solid (28.0 g, 99%). 1H NMR (300 MHz, CDCl3) δ 12.12 (s, 1H), 7.78 (s, 1H), 7.31 (s, 1H), 2.62 (s, 3H).

後処理

  1. temperatureThe reaction was heated
  2. temperatureto reflux
  3. temperatureAfter heating for 1 h
  4. additionpoured over ice
  5. extractionThe slurry was extracted with ethyl acetate 3×
  6. washthe combined organic layer was washed with brine
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-f0f7c87820114e84b606c4a4a374221e
出典データセット
uspto-grants-2016_04
特許番号
US09309251B2

反応ノート

読み込み中…