Reaktion #1537221

ord-5c79e0b3434342ea8430fc51f22ef561

Reaktionsgleichung

O=C1C=C(O)C(=O)C=C1O
2,5-Dihydroxy-1,4-benzoquinone
Cl
HCl
CC(C)=O
acetone
CC1(C)Oc2cc3c(cc2O1)OC(C)(C)O3
P2O5
CC1(C)Oc2cc3c(cc2O1)OC(C)(C)O3
2,2,6,6-Tetramethylbenzo[1,2-d:4,5-d']bis(1,3)dioxole
Oc1cc(O)c(O)cc1O
1,2,4,5-Tetrahydroxybenzene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe solution was filtered
  2. 2
    Sonstigethe solution evaporated to dryness
  3. 3
    SonstigeThe product was isolated as a grey brown powder

Vorschrift

2,5-Dihydroxy-1,4-benzoquinone (10.00 g, 71.43 mmol) was suspended in water (200 ml, distilled) followed by HCl (6 mL, 142.86 mmol, conc.). Iron (4.00 g, 71.43 mmol, powder) was added and the mixture was stirred 30 minutes at room temperature. The solution was filtered and the solution evaporated to dryness. The product was isolated as a grey brown powder containing some iron complexes. Yield 14.80 g. The product is used as such in the reaction with acetone and P2O5 (Example 5) with no negative effects.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05599522uspto-grants-1997_02