Hydrochloric Acid → 7-Methoxy-2-methylbenzofuran

HRID 1091857Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1091857
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH2:10][CH:11]=C.[F-].[Cs+].Cl.[C:16](OCC)(=O)C>C(N(CC)C1C=CC=CC=1)C>[CH3:1][O:2][C:3]1[C:4]2[O:9][C:10]([CH3:11])=[CH:16][C:5]=2[CH:6]=[CH:7][CH:8]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
217.5 °C

Versuchsvorschrift

To a well stirred solution of 1-methoxy-2-(2-propenyloxy)benzene (118.0 g, 0.728 moles) in N,N-diethyl aniline (1.0 L) was added cesium fluoride (134 g, 0.874 mmoles) and the mixture was heated to 215-220° C. for 4-5 hours. Reaction mixture was cooled to room temperature and 10% aqueous HCl solution (3.0 lit) was added followed by addition of ethyl acetate (2.0 L). The mixture was the filtered through Celite bed. The organic layer was separated and washed with water (2×1.0 L) and dried over anhydrous sodium sulfate. Removal of solvent under vacuo gave crude product (72.0 g) as dark brown oil. It was then purified through silica gel column using petroleum ether: ethyl acetate (9:1) as an eluent to afford the product as pale yellow oil (4.6 g).

Aufarbeitung

  1. customReaction mixture
  2. temperaturewas cooled to room temperature
  3. filtrationfiltered through Celite bed
  4. customThe organic layer was separated
  5. washwashed with water (2×1.0 L)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customRemoval of solvent under vacuo
  8. customgave crude product (72.0 g) as dark brown oil
  9. customIt was then purified through silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-c4fc5bde12514cea9c9a726da44093a9
Quelldatensatz
uspto-grants-2012_03
Patentnummer
US08129401B2

Notizen zur Reaktion

Wird geladen…