Sulfuric Acid → 2H-1-Benzopyran-6-ol, 3,4-dihydro-2-methoxy-2,5,7,8-tetramethyl-

HRID 263924

Reaktionsgleichung

Reaktionsgleichung von HRID 263924
S(=O)(=O)(O)O.[CH:6](OC)(OC)OC.[CH3:13][C:14]1[C:15]([OH:23])=[C:16]([CH3:22])[C:17]([CH3:21])=[C:18]([CH:20]=1)[OH:19].[CH:24]([C:26]([CH3:28])=[O:27])=[CH2:25]>CO.C(OCC)C>[OH:23][C:15]1[C:14]([CH3:13])=[C:20]2[C:18](=[C:17]([CH3:21])[C:16]=1[CH3:22])[O:19][C:26]([O:27][CH3:6])([CH3:28])[CH2:24][CH2:25]2

Komponenten

7

Versuchsvorschrift

Concentrated sulfuric acid (0.8 mL) was added dropwise to a solution of trimethyl orthoformate (Aldrich, 48.5 g, 457.0 mmol) and trimethyl hydroquinone (Aldrich, 50.0 g, 328.5 mol) in methanol (200 mL), cooled by a water/ice bath. Methyl vinyl ketone (Aldrich, 46.05 g, 657.0 mmol) was added slowly (1.5 h) to the reaction mixture while the reaction mixture was cooled by an ice/water bath. A pasty slurry formed. The reaction mixture was allowed to come to ambient temperature and was stirred at ambient temperature for 48 h. The reaction mixture was diluted with diethyl ether (600 mL) and the resulting solution was extracted with water (2×200 mL) and saturated aqueous sodium bicarbonate (2×100 mL). The organic solution was dried (sodium sulfate) and concentrated in vacuo to give a tan solid. The solid was recrystallized from methanol to give 71.8 g (92.6%) of the desired product as a tan solid.

Aufarbeitung

  1. temperaturecooled by a water/ice bath
  2. temperaturewas cooled by an ice/water bath
  3. customA pasty slurry formed
  4. customto come to ambient temperature
  5. extractionthe resulting solution was extracted with water (2×200 mL) and saturated aqueous sodium bicarbonate (2×100 mL)
  6. dry with materialThe organic solution was dried (sodium sulfate)
  7. concentrationconcentrated in vacuo
  8. customto give a tan solid
  9. customThe solid was recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-e869cbf248364ce393243da6e7bfa8b3
Quelldatensatz
uspto-grants-1997_07
Patentnummer
US05646149

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