Sodium Hydroxide → 3,5-Dimethoxy-2-methylbenzoic acid

HRID 1384332ノート

反応式

HRID 1384332 の反応式
[CH3:1][O:2][C:3]1[C:4]([CH3:15])=[C:5]([CH:10]=[C:11]([O:13][CH3:14])[CH:12]=1)[C:6]([O:8]C)=[O:7].[OH-].[Na+]>CO>[CH3:1][O:2][C:3]1[C:4]([CH3:15])=[C:5]([CH:10]=[C:11]([O:13][CH3:14])[CH:12]=1)[C:6]([OH:8])=[O:7]

参加物

4

実験手順

Solid methyl 3,5-dimethoxy-2-methylbenzoate (5.83 g, J. C. S. Perkin I, 1973, 2853.) was dissolved in methanol (80 ml). A solution of aqueous sodium hydroxide (10%, 80 ml) was added and the solution stirred at room temperature for 1 hour. The reaction was then concentrated under reduced pressure to approximately half of the original volume before adding aqueous hydrochloric acid (200 ml). The white precipitate that formed was extracted with ethyl acetate (2×250 ml). The combined extracts were dried over anhydrous magnesium sulphate, filtered and concentrated under reduced pressure to give the sub-title compound as a colourless solid (5.41 g).

後処理

  1. concentrationThe reaction was then concentrated under reduced pressure to approximately half of the original volume
  2. additionbefore adding aqueous hydrochloric acid (200 ml)
  3. customThe white precipitate that formed
  4. extractionwas extracted with ethyl acetate (2×250 ml)
  5. dry with materialThe combined extracts were dried over anhydrous magnesium sulphate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-4e8ba86960b2481cac3204b35734007a
出典データセット
uspto-grants-2001_07
特許番号
US06258838B1

反応ノート

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