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Pyridine → 5,6-Dihydroxy-4-nitro-2-benzofuran-1,3-dione

HRID 1881210
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1881210
[OH:1][C:2]1[C:3]([N+:15]([O-:17])=[O:16])=[C:4]2[C:8](=[CH:9][C:10]=1[O:11]C)[C:7](=[O:13])[O:6][C:5]2=[O:14].[Cl-].[Al+3].[Cl-].[Cl-].N1C=CC=CC=1>C(OCC)(=O)C>[OH:1][C:2]1[C:3]([N+:15]([O-:17])=[O:16])=[C:4]2[C:8](=[CH:9][C:10]=1[OH:11])[C:7](=[O:13])[O:6][C:5]2=[O:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 6451240Aluminum(III) ChlorideHCID 866334455-Hydroxy-6-methoxy-4-nitro-isobenzofuran-1,3-dione

Produkt 1

HCID 159832305,6-Dihydroxy-4-nitro-2-benzofuran-1,3-dione

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel2×

Versuchsvorschrift

5-Hydroxy-6-methoxy-4-nitro-isobenzofuran-1,3-dione (115 mg), aluminum chloride (80 mg) was mixed with ethyl acetate (3 ml). Pyridine (155 μl) in ethyl acetate (2 ml) was added dropwise. The resulting mixture was stirred at room temperature for 0.5 hours, heated to reflux for 3 hours, and then quenched with water (0.5 ml) and conc. HCl (0.5 ml) at 60° C. Ethyl acetate and water was removed in vacuo. The remainder was mixed with brine (2 ml) and extracted two times with ethyl acetate (15 ml). The combined organic layers were dried over anhydrous Na2SO4, filtrated, evaporated and triturated with diethyl ether.

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for 3 hours
  3. customquenched with water (0.5 ml) and conc. HCl (0.5 ml) at 60° C
  4. customEthyl acetate and water was removed in vacuo
  5. additionThe remainder was mixed with brine (2 ml)
  6. extractionextracted two times with ethyl acetate (15 ml)
  7. dry with materialThe combined organic layers were dried over anhydrous Na2SO4
  8. filtrationfiltrated
  9. customevaporated
  10. customtriturated with diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-f8a916d1eb674a33968be81d16f22307
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08318785B2

Notizen zur Reaktion

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