Potassium Carbonate → HCID 13723675, Verbindung

HRID 1448965Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1448965
[CH3:1][C:2]1[CH:3]=[C:4]([OH:10])[C:5](=[CH:7][C:8]=1[CH3:9])[OH:6].C(=O)([O-])[O-].[K+].[K+].Br[C:18](Br)([CH3:24])[C:19]([O:21][CH2:22][CH3:23])=[O:20]>CC(C)=O>[CH3:1][C:2]1[C:8]([CH3:9])=[CH:7][C:5]2[O:6][CH:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:24][O:10][C:4]=2[CH:3]=1

Komponenten

5

Versuchsvorschrift

A stirred solution of 4,5-dimethylcatechol (7.0 g.) in dry acetone (45 ml.) was heated under reflux, then potassium carbonate (5 g.) was added followed by the dropwise addition of ethyl dibromopropionate (3.5 g.). The addition procedure was repeated a further three times over 11/4 hours then the reaction was stirred under reflux for a further 33/4 hours. After cooling, the mixture was filtered, the solids washed well with acetone then the combined filtrate concentrated in vacuo. Water (35 ml.) was added, the resulting solid collected, washed with petrol then taken up in ether. The ethereal solution was washed with water, dried (Na2SO4) and evaporated in vacuo to give ethyl 6,7-dimethyl-1,4-benzodioxan-2-carboxylate (10.17 g.), m.p. 70°-71° C.

Aufarbeitung

  1. temperatureunder reflux
  2. additionThe addition procedure
  3. custom4 hours
  4. temperatureunder reflux for a further 33/4 hours
  5. temperatureAfter cooling
  6. filtrationthe mixture was filtered
  7. washthe solids washed well with acetone
  8. concentrationthe combined filtrate concentrated in vacuo
  9. additionWater (35 ml.) was added
  10. customthe resulting solid collected
  11. washwashed with petrol
  12. washThe ethereal solution was washed with water
  13. dry with materialdried (Na2SO4)
  14. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-dd7618234cba4d3ea4d9b913834d861f
Quelldatensatz
uspto-grants-1980_02
Patentnummer
US04188390

Notizen zur Reaktion

Wird geladen…