Reaktion #4979

ord-97f438e7ffbd4764b1ee7bf05860487d

Reaktionsgleichung

Cc1ccc(O)cc1O
4-Methylresorcinol
O=C1CCC(=O)O1
succinic anhydride
Cc1cc2c(cc1O)Oc1cc(O)c(C)cc1C2=CCC(=O)O
powder
Ausbeute 74.2%
Cc1cc2c(cc1O)Oc1cc(O)c(C)cc1C2=CCC(=O)O
9-Carboxyethylidene-3,6-dihydroxy-2,7-dimethyl-9H-xanthene
Ausbeute 74.2%

Reaktionsbedingungen

Temperatur
65°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe flask was purged with nitrogen
  2. 2
    workup.ADDITIONMethanesulfonic acid (150 mL) was added
  3. 3
    workup.ADDITIONThe solution was added dropwise to 1 L
  4. 4
    Temperaturice-cooled water
  5. 5
    workup.ADDITIONwith the simultaneous addition of 50% aq sodium hydroxide
  6. 6
    Temperaturto maintain the pH at 2.25 +/-0.25
  7. 7
    SonstigeThe product was collected by centrifugation
  8. 8
    Waschenwashed with water (3×) and acetone (2×)
  9. 9
    SonstigeThe solid was air-dried
  10. 10
    Sonstigevacuum-dried at 110° C.

Vorschrift

4-Methylresorcinol (25.8 g, 0.208 mol) and succinic anhydride (20.8 g, 0.208 g) were placed in a round bottom flask and the flask was purged with nitrogen. Methanesulfonic acid (150 mL) was added and the solution heated under nitrogen to 65° C. for 2 hours. The solution was added dropwise to 1 L of rapidly stirred, ice-cooled water with the simultaneous addition of 50% aq sodium hydroxide to maintain the pH at 2.25 +/-0.25. The product was collected by centrifugation and washed with water (3×) and acetone (2×). The solid was air-dried, then vacuum-dried at 110° C. to afford a brick-red powder (24.1 g, 74%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05242796uspto-grants-1993_09