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

HRID 1453239
ノート
印刷プレビュー

反応式

HRID 1453239 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, 1H), 7.51 (dd, J=8.6, 2.3 Hz, 1H), 7.66 (d, J=2.3 Hz, 1H).

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-82bbd7acc51948138bc8156dcf06567f
出典データセット
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07473790B2

反応ノート

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