StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Benzene → 2-Nitroxymethylpyridine nitrate

HRID 1719515
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1719515
[N+:1]([O-:4])([OH:3])=[O:2].C(OC(=O)C)(=O)C.[N+:12]([O-:15])([OH:14])=[O:13].O[CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=1.C1C=CC=CC=1>CCCCCC>[N+:1]([O-:4])([OH:3])=[O:2].[O:13]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=1)[N+:12]([O-:15])=[O:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 241BenzeneHCID 944Nitric AcidHCID 7918Acetic AnhydrideHCID 70400506HCID 70400506, Verbindung

Produkt 1

HCID 867402952-Nitroxymethylpyridine nitrate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058HexaneLösungsmittel

Versuchsvorschrift

Fuming nitric acid (4.1 ml) was added dropwise to acetic anhydride (13.5 ml) with stirring at 5° to 10° C. After the mixture was stirred for 30 minutes at 5° C., 2-hydroxymethylpyridine nitrate (3.3 g) was added in some portions thereto. The resulting mixture was stirred for 3 hours at 0° to 5° C. A mixture of benzene (15 ml) and n-hexane (30 ml) was added thereto. The mixture formed two layers. The upper layer was separated and discarded while the remaining lower layer was again treated with a mixture of benzene (10 ml) and n-hexane (10 ml). After the separation of the layers, the lower layer was again separated, mixed with benzene (10 ml) and made homogeneous with isopropyl alcohol (10 ml). The resulting mixture was allowed to stand overnight in a refrigerator to give crystals. The crystals were collected by filtration and washed with diethyl ether to give white crystals of 2-nitroxymethylpyridine nitrate (2.4 g), mp. 75° to 77° C.

Aufarbeitung

  1. stirringAfter the mixture was stirred for 30 minutes at 5° C.
  2. stirringThe resulting mixture was stirred for 3 hours at 0° to 5° C
  3. additionwas added
  4. customThe mixture formed two layers
  5. customThe upper layer was separated
  6. additionwas again treated with a mixture of benzene (10 ml) and n-hexane (10 ml)
  7. customAfter the separation of the layers
  8. customthe lower layer was again separated
  9. additionmixed with benzene (10 ml)
  10. customto give crystals
  11. filtrationThe crystals were collected by filtration
  12. washwashed with diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-10a159dfdc554b0e9bf8618e2e3940c8
Quelldatensatz
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04540701

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion