Ethanol → 4,5-Dimethoxy-2-(4-methylthiophenyl)benzaldehyde

HRID 2416592

반응식

HRID 2416592 반응식
Br[C:2]1[C:9]([O:10][CH3:11])=[C:8]([O:12][CH3:13])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[CH3:14][S:15][C:16]1[CH:21]=[CH:20][C:19](B(O)O)=[CH:18][CH:17]=1.C(=O)([O-])[O-].[Na+].[Na+].C(O)C>C1(C)C=CC=CC=1.O>[CH3:13][O:12][C:8]1[C:9]([O:10][CH3:11])=[CH:2][C:3]([CH:4]=[O:5])=[C:6]([C:19]2[CH:20]=[CH:21][C:16]([S:15][CH3:14])=[CH:17][CH:18]=2)[CH:7]=1

참가 물질

7

반응물 4

HCID 702EthanolHCID 10340Sodium CarbonateHCID 6185382-Bromo-3,4-dimethoxybenzaldehydeHCID 27339594-(Methylthio)phenylboronic acid

생성물 1

HCID 113920804,5-Dimethoxy-2-(4-methylthiophenyl)benzaldehyde수율 85%

시약·촉매·용매 2

HCID 962Water용매HCID 1140Toluene용매

실험 절차

2-Bromoveratraldehyde (25 g, 103.3 mmol) and 4-(methylthio)benzeneboronic acid (19.66 g, 118.5 mmol) were dissolved in toluene (550 mL) and sodium carbonate (2M, 103 μL, 206 mmol) was added. To this reaction mixture was added ethanol (50 mL) followed by tetrakis (triphenylphosphine)palladium (3.4 g, 2.5 mmol) and the reaction mixture was refluxed overnight under nitrogen atmosphere. The reaction mixture was cooled to room temperature, diluted with water (250 mL) and extracted with ethyl acetate (2×250 mL). The combined organic extracts were washed with water (4×250 mL), brine (1×250 mL), dried over sodium sulfate, filtered and the filtrate was evaporated under reduced pressure to give the crude product. The product was purified by trituration with ethyl acetate/hexane to give the title compound as a white solid (21.3 g, 85% yield), mp 114-115° C. 1H NMR (CDCl3, 300 MHz) δ 9.83 (s, 1H), 7.64 (s, 1H), 7.43-7.23 (m, 4H), 6.83 (s, 1H), 3.98 (d, J=2.4 Hz, 6H), 2.55 (s, 3H). 13C NMR (CDCl3, 75.45 MHz) δ 190.9, 153.4, 148.7, 1408, 138.9, 134.5, 134.1, 130.5, 130.1, 128.0, 128.0, 126.9, 126.1, 112.5, 108.7, 56.2, 56.1, 15.6. LRMS (APIMS) m/z 289 (M+H)+.

후처리

  1. temperaturethe reaction mixture was refluxed overnight under nitrogen atmosphere
  2. extractionextracted with ethyl acetate (2×250 mL)
  3. washThe combined organic extracts were washed with water (4×250 mL), brine (1×250 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customthe filtrate was evaporated under reduced pressure
  7. customto give the crude product
  8. customThe product was purified by trituration with ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-37e15bee1d2b488ea0e7f19945ea824b
출처 데이터셋
uspto-grants-2004_11
특허 번호
US06825185B2

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