Nitric Acid → HCID 19045274, Verbindung

HRID 1591167Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1591167
[CH3:1][N:2]1[CH2:7][CH2:6][C:5]2([CH2:12][C:11](=[O:13])[C:10]3[CH:14]=[CH:15][CH:16]=[CH:17][C:9]=3[O:8]2)[CH2:4][CH2:3]1.[N+:18]([O-])([OH:20])=[O:19].C(OCC)(=O)C.C(=O)(O)[O-].[Na+]>S(=O)(=O)(O)O>[CH3:1][N:2]1[CH2:7][CH2:6][C:5]2([CH2:12][C:11](=[O:13])[C:10]3[CH:14]=[C:15]([N+:18]([O-:20])=[O:19])[CH:16]=[CH:17][C:9]=3[O:8]2)[CH2:4][CH2:3]1

Komponenten

6

Edukt 4

HCID 944Nitric Acid2×HCID 8857Ethyl AcetateHCID 516892Sodium BicarbonateHCID 1233903N-methylspiro[2H-1-benzopyran-2,4'-piperidine]4(3H)-one

Produkt 1

HCID 19045274HCID 19045274, VerbindungAusbeute 77 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Sulfuric acid (55 ml) was cooled to 0° C. and was stirred as 3,4-dihydro-1'-methyl-spiro[2H-1-benzopyran-2,4'-piperidin]-4-one (11.56 g, 0.05 mol) was added over 20 minutes. Some gum separated. A solution of 90% nitric acid (2.5 ml, 0.0525 mol) in sulfuric acid (5 ml) was added over 20 minutes. The mixture was stirred for 2 hours at 0° C. and then for 1 hour at room temperature. A solution resulted but nitration was not complete. 90% Nitric acid (0.3 ml, 0.007 mol) was added and stirring was continued for 11/2 hours at room temperature. The reaction solution was poured into a mixture of ice, ethyl acetate, and sodium bicarbonate (210 g). The basic mixture was filtered, the ethyl acetate layer was separated and the aqueous layer was extracted with ethyl acetate (150 ml). The combined ethyl acetate extracts were washed with saturated NaCl, dried, filtered and concentrated in vacuo to yield 10.6 g (77%) of product

Aufarbeitung

  1. additionwas added over 20 minutes
  2. customSome gum separated
  3. waitfor 1 hour at room temperature
  4. customA solution resulted
  5. stirringstirring
  6. custom2 hours
  7. customat room temperature
  8. filtrationThe basic mixture was filtered
  9. customthe ethyl acetate layer was separated
  10. extractionthe aqueous layer was extracted with ethyl acetate (150 ml)
  11. washThe combined ethyl acetate extracts were washed with saturated NaCl
  12. customdried
  13. filtrationfiltered
  14. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-e2750eb075b34226829a49716d012c76
Quelldatensatz
uspto-grants-1993_04
Patentnummer
US05206240

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