Reaktion #41218

ord-ba0d0475fac4495ead26baa58c66eb98

Reaktionsgleichung

ClCCl
dichloromethane
O=C(O)c1cc(O)c2c(c1)C(=O)c1cccc(O)c1C2=O
4,5-Dihydroxy-9,10-dioxoanthracene-2-carboxylic acid
O=C(Cl)COCc1ccccc1
Benzyloxyacetyl chloride
O
water
CCOC(C)=O
ethyl acetate
O=C(COCc1ccccc1)Oc1cccc2c1C(=O)c1c(OC(=O)COCc3ccccc3)cc(C(=O)O)cc1C2=O
4,5-Bis(2-benzyloxyacetyloxy)-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto give a clear reaction mixture which
  2. 2
    workup.STIRRINGwas stirred at RT over the weekend
  3. 3
    Sonstigequenched with 2M HCl (200 ml)
  4. 4
    SonstigeAn orange solid was isolated by filtration
  5. 5
    SonstigeA yellow solid was isolated by filtration (3.6 g, 61%)

Vorschrift

4,5-Dihydroxy-9,10-dioxoanthracene-2-carboxylic acid (3.0 g) was suspended in pyridine (100 ml) and stirred at RT for 30 mins. Benzyloxyacetyl chloride (3.6 g, 5 equiv.) was added, to give a clear reaction mixture which was stirred at RT over the weekend. The reaction mixture was reduced to a smaller volume and quenched with 2M HCl (200 ml), adjusting the pH to pH 2. An orange solid was isolated by filtration. This crude solid was slurried in water (30 ml), followed by ethyl acetate (30 ml) and dichloromethane (30 ml). A yellow solid was isolated by filtration (3.6 g, 61%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728035B2uspto-grants-2010_06