Methanol → Benzoic acid, 2-hydroxy-4-methyl-, methyl ester

HRID 356741

반응식

HRID 356741 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([OH:11])[C:5](=[CH:9][CH:10]=1)[C:6]([OH:8])=[O:7].S(=O)(=O)(O)O.[CH3:17]O>>[CH3:1][C:2]1[CH:3]=[C:4]([OH:11])[C:5](=[CH:9][CH:10]=1)[C:6]([O:8][CH3:17])=[O:7]

참가 물질

4

실험 절차

4-Methylsalicylic acid (100 g, 658 mmoles) was dissolved in anhydrous methanol (500 mL) and concentrated sulfuric acid (25 mL) was added carefully. The solution was refluxed for 18 hours, then cooled to room temperature. The reaction mixture was concentrated to about 150 mL, and ethyl acetate (250 mL) was added. The ethyl acetate solution was washed twice with saturated aqueous sodium bicarbonate (250 mL portions) and then with saturated aqueous sodium chloride (100 mL). The ethyl acetate solution was dried over anhydrous sodium sulfate, filtered, and evaporated to a clear, reddish-brown liquid. This crude product was vacuum distilled (oil pump) to afford a clear, viscous liquid that solidified on standing to afford 98.1 g (90% yield) of methyl 4-methylsalicylate.

후처리

  1. temperatureThe solution was refluxed for 18 hours
  2. concentrationThe reaction mixture was concentrated to about 150 mL, and ethyl acetate (250 mL)
  3. additionwas added
  4. washThe ethyl acetate solution was washed twice with saturated aqueous sodium bicarbonate (250 mL portions)
  5. dry with materialThe ethyl acetate solution was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customevaporated to a clear, reddish-brown liquid
  8. distillationdistilled (oil pump)
  9. customto afford a clear, viscous liquid that solidified

출처 및 근거

ORD 기록
ord-a8dc5e8b7a0d4afeb03740b0c86d7cf0
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05837878

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