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Triethylsilane → 3-(4-Bromo-3,5-dimethylphenyl)-2,5-dihydrofuran

HRID 237582
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반응식

HRID 237582 반응식
C([SiH](CC)CC)C.[Br:8][C:9]1[C:14]([CH3:15])=[CH:13][C:12]([C:16]2[CH:20]=[CH:19][O:18][CH:17]=2)=[CH:11][C:10]=1[CH3:21].C([O-])(O)=O.[Na+]>FC(F)(F)C(O)=O>[Br:8][C:9]1[C:14]([CH3:15])=[CH:13][C:12]([C:16]2[CH2:17][O:18][CH2:19][CH:20]=2)=[CH:11][C:10]=1[CH3:21]
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참가 물질

5

반응물 3

HCID 12052TriethylsilaneHCID 516892Sodium BicarbonateHCID 866972453-(4-Bromo-3,5-dimethylphenyl)furan

생성물 1

HCID 866972463-(4-Bromo-3,5-dimethylphenyl)-2,5-dihydrofuran

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

Triethylsilane (3.67 mL) is added dropwise to a solution of 3-(4-bromo-3,5-dimethylphenyl)furan (580 mg) in trifluoroacetic acid and the resulting mixture is stirred at room temperature for 3 h. Saturated aqueous NaHCO3 solution is added and the aqueous phase is separated and extracted with ethyl acetate. The combined extracts are washed with brine, dried over MgSO4 and concentrated in vacuo. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 95:5) to give the title compound. LC (method 9): tR=1.16 min; Mass spectrum (ESI+): m/z=251, 253 [M+H]+.

후처리

  1. customthe aqueous phase is separated
  2. extractionextracted with ethyl acetate
  3. washThe combined extracts are washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customThe residue is chromatographed on silica gel (cyclohexane/ethyl acetate 95:5)

출처 및 근거

ORD 기록
ord-1bfc0fa76d704a7da2e2c263c18761b5
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642585B2

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