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Methanol → (S)-3-(4-bromophenyl)cyclopentanone oxime

HRID 2404368
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HRID 2404368 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[CH2:12][CH2:11][C:10](=O)[CH2:9]2)=[CH:4][CH:3]=1.CO.C([O-])(=O)C.[Na+].Cl.[NH2:22][OH:23]>CC(OC)(C)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[CH2:12][CH2:11][C:10](=[N:22][OH:23])[CH2:9]2)=[CH:4][CH:3]=1
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참가 물질

6

반응물 4

HCID 887MethanolHCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 25002103(S)-3-(4-Bromophenyl)cyclopentan-1-one

생성물 1

HCID 86671372(S)-3-(4-bromophenyl)cyclopentanone oxime수율 95.2%

시약·촉매·용매 1

HCID 15413tert-Butyl methyl ether
용매

실험 절차

A slurry of (S)-3-(4-bromophenyl)cyclopentanone (prepared according to J. Org. Chem., 2009, 74, 929; 10.9 g, 45.5 mmol), MeOH (110 mL), sodium acetate (5.59 g, 68.2 mmol), and hydroxylamine hydrochloride (4.74 g, 68.2 mmol) was stirred at room temperature. After 10 minutes, LCMS showed complete reaction. Diluted with MTBE (300 mL) and washed with water (100 mL) and brine (50 mL). The organic layer was dried (Na2SO4), filtered, and concentrated. The residue was purified by silica gel chromatography (gradient elution, 25-50% EtOAc/hexanes) to afford the title compound (11.0 g, 43.3 mmol, 95%). MS (DCI) m/z 254 (M+H)+.

후처리

  1. customreaction
  2. washwashed with water (100 mL) and brine (50 mL)
  3. dry with materialThe organic layer was dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by silica gel chromatography (gradient elution, 25-50% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-1b061fa03ab84f1db8c8abc4bdbe0663
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802711B2

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