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Cornforth reagent → 1-(5-Bromo-2-chlorophenyl)ethan-1-one

HRID 858785
ノート
印刷プレビュー

反応式

HRID 858785 の反応式
[Cr](O[Cr]([O-])(=O)=O)([O-])(=O)=O.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[Br:22][C:23]1[CH:24]=[CH:25][C:26]([Cl:32])=[C:27]([CH:29]([OH:31])[CH3:30])[CH:28]=1>C(Cl)Cl>[Br:22][C:23]1[CH:24]=[CH:25][C:26]([Cl:32])=[C:27]([C:29](=[O:31])[CH3:30])[CH:28]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 2724130Cornforth reagent2 回HCID 587626441-(5-Bromo-2-chlorophenyl)ethanol

生成物 1

HCID 136281451-(5-Bromo-2-chlorophenyl)ethan-1-one収率 85.7%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Pyridinium dichromate (2.6 g, 6.94 mmol) was added to a solution of 1-(5-bromo-2-chloro-phenyl)-ethanol (1.09 g, 4.6 mmol) in CH2Cl2 (20 mL). The reaction was stirred for 15 hours and then more pyridinium dichromate (2.6 g, 6.94 mmol) was added. After another 24 hours celite was added and the mixture was stirred for 20 mins. The reaction mixture was filtered through a pad of celite washing with ether. The filtrate was concentrated to a brown oil. The residue was purified by flash silica gel chromatography (0% to 10% EtOAc in hexanes) to give the title compound as a clear oil (0.92 g, 85%). 1H NMR (400 MHz, CDCl3): δ 2.64 (s, 3H), 7.29 (d, J=8.6 Hz, 1 H), 7.51 (dd, J=8.6, 2.3 Hz, 1 H), 7.66 (d, J=2.3 Hz, 1 H).

後処理

  1. additionAfter another 24 hours celite was added
  2. stirringthe mixture was stirred for 20 mins
  3. filtrationThe reaction mixture was filtered through a pad of celite
  4. washwashing with ether
  5. concentrationThe filtrate was concentrated to a brown oil
  6. customThe residue was purified by flash silica gel chromatography (0% to 10% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-27319599dd4f4126a9a17fd23917cf76
出典データセット
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07148226B2

反応ノート

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