Acetic Anhydride → 6-Methyl-2-oxo-2H-1-benzopyran-7-yl acetate

HRID 359502Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 359502
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[O:8][C:7](=[O:13])[CH:6]=[CH:5]2.[C:14](OC(=O)C)(=[O:16])[CH3:15].C(O[Na])(C)=O>O>[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[O:12][C:14](=[O:16])[CH3:15])[O:8][C:7](=[O:13])[CH:6]=[CH:5]2

Komponenten

5

Edukt 3

HCID 7918Acetic AnhydrideHCID 54129132H-1-Benzopyran-2-one, 7-hydroxy-6-methyl-HCID 178418247HCID 178418247, Verbindung

Produkt 1

HCID 132989326-Methyl-2-oxo-2H-1-benzopyran-7-yl acetate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Versuchsvorschrift

To prepare the alkylangelicins with an alkyl group in the 4'-position of the furan ring, the suitable umbelliferones, (I), (II), (III) were acetylated and the 7-acetoxycoumarins thus obtained were submitted to the Fries rearrangement. The 8-acetylumbelliferones were converted into the ethyl esters of the 7-(8-acetylcoumarinyl)oxyacetic acids, which were then hydrolized and cyclized yielding the desired 4'-methylangelicins. In such a manner a mixture of 6-methyl-7-hydroxycoumarin (I) (10.0 g), acetic anhydride (40 ml) and anhydrous AcONa (4.0 g) was refluxed for 1 h. To the reaction mixture an equal volume of H2O was cautiously added and the whole was refluxed for 10 min. The mixture was diluted with H2O (300 ml), chilled and the precipitate was collected by filtration, washed several times with H2O, dried and crystallized from MeOH, yielding the 6-methyl-7-acetoxycoumarin (XXII) (10.0 g; m.p. 147° C.). ##STR28##

Aufarbeitung

  1. customhydrolized and cyclized yielding the desired 4'-methylangelicins
  2. temperaturewas refluxed for 1 h
  3. temperaturethe whole was refluxed for 10 min
  4. temperaturechilled
  5. filtrationthe precipitate was collected by filtration
  6. washwashed several times with H2O
  7. customdried
  8. customcrystallized from MeOH

Quellen und Nachweise

ORD-Eintrag
ord-06eb8eaed64346a996d272bbc2cd30f9
Quelldatensatz
uspto-grants-1991_03
Patentnummer
US05001147

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