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HCID 58762226, 화합물 → 1-(4-Methoxyphenyl)pentan-3-one

HRID 1453018
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HRID 1453018 반응식
[CH2:1]([Mg]Br)[CH3:2].CON(C)[C:8](=[O:19])[CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=1>C1COCC1>[CH3:18][O:17][C:14]1[CH:15]=[CH:16][C:11]([CH2:10][CH2:9][C:8](=[O:19])[CH2:1][CH3:2])=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 58762226HCID 58762226, 화합물HCID 178418443HCID 178418443, 화합물

생성물 1

HCID 2281241-(4-Methoxyphenyl)pentan-3-one수율 50%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Ethylmagnesium bromide (10.8 mL, 10.8 mmol, 1M soln in THF) was added to a cooled −78° C. solution of N-Methoxy-3-(4-methoxy-phenyl)-N-methyl-propionamide (2 g, 8.96 mmol, from Step 1) dissolved in THF (20 mL). The reaction mixture was stirred for 60 min. The reaction was quenched with saturated NH4Cl and extracted with EtOAc. The organic layer was washed brine, dried over Na2SO4 and concentrated to a clear oil. The residue was purified by silica gel chromatography (5% EtOAc in hexanes) to give the title compound as a clear oil (0.87 g, 50%).

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후처리

  1. customThe reaction was quenched with saturated NH4Cl
  2. extractionextracted with EtOAc
  3. washThe organic layer was washed brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated to a clear oil
  6. customThe residue was purified by silica gel chromatography (5% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-592ecd34c6dd4414883a837a6e500df5
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07473790B2

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