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

HRID 49179

反応式

HRID 49179 の反応式
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

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 1140Toluene溶媒

実験手順

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 mL, 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) δ9.83 (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) δ190.9, 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)+.

後処理

  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

出典と根拠

ORDレコード
ord-12d70e5dc7a843fcae2bd945d35205be
出典データセット
uspto-grants-2004_03
特許番号
US06706724B2

関連ノート

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