Iodoethane → 3,4-Dimethoxy-5-ethoxybenzoic Acid

HRID 2230660Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2230660
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([OH:14])[C:11]=1[O:12][CH3:13])[C:6]([OH:8])=[O:7].C(=O)([O-])[O-].[K+].[K+].[CH2:21](I)[CH3:22].[OH-].[K+]>CC(C)=O.C(O)C.O.CO>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:9]=[C:10]([O:14][CH2:21][CH3:22])[C:11]=1[O:12][CH3:13])[C:6]([OH:8])=[O:7]

Komponenten

9

Versuchsvorschrift

Combine 3,4-dimethoxy-5-hydroxybenzoic acid (1.0 g, 5.0 mmol), potassium carbonate (4.2 g, 30.2 mmol), and ethyl iodide (3.9 g, 25.2 mmol) in acetone (50 mL). Heat to reflux. After 24 hours, cool, add methanol (25 mL) and water (5 mL) After 18 hours, concentrate in vacuo to give a residue. Combine the residue and ethanol (50 mL) and potassium hydroxide (0.56 g, 10 mmol). After 18 hours, concentrate in vacuo to give a residue. Partition the residue between ethyl acetate and a 1 M aqueous solution of hydrochloric acid. Extract the aqueous layer three times with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and concentrate in vacuo to give a residue. Triturate the residue to give a solid. Collect the solid to give the title compound.

Aufarbeitung

  1. temperatureHeat to reflux
  2. temperaturecool
  3. concentrationconcentrate in vacuo
  4. customto give a residue
  5. waitAfter 18 hours
  6. concentrationconcentrate in vacuo
  7. customto give a residue
  8. customPartition the residue between ethyl acetate
  9. extractionExtract the aqueous layer three times with ethyl acetate
  10. dry with materialdry over Na2SO4
  11. filtrationfilter
  12. concentrationconcentrate in vacuo
  13. customto give a residue
  14. customTriturate the residue
  15. customto give a solid
  16. customCollect the solid

Quellen und Nachweise

ORD-Eintrag
ord-26adde2b9cf14205b7f93834ec5614d6
Quelldatensatz
uspto-grants-2002_07
Patentnummer
US06423704B1

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