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

HRID 858785
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반응식

HRID 858785 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2724130Cornforth reagent2회HCID 587626441-(5-Bromo-2-chlorophenyl)ethanol

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-27319599dd4f4126a9a17fd23917cf76
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07148226B2

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