Potassium Carbonate → 2-[(2-Chloro-4-nitrophenoxy)methyl]-6-methylpyridine

HRID 877087Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 877087
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1F.C([O-])([O-])=O.[K+].[K+].[CH3:18][C:19]1[N:24]=[C:23]([CH2:25][OH:26])[CH:22]=[CH:21][CH:20]=1>CC(C)=O>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[O:26][CH2:25][C:23]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:18])[N:24]=1

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 676882-Chloro-1-fluoro-4-nitrobenzeneHCID 707366-Methyl-2-pyridylmethanol

Produkt 1

HCID 668773902-[(2-Chloro-4-nitrophenoxy)methyl]-6-methylpyridineAusbeute 68,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

To a solution of 2-chloro-1-fluoro-4-nitro-benzene (8.75 g, 50 mmol) in dry acetone (100 ml) was added 10.0 g of K2CO3 and 6.15 g of 6-methyl-2-pyridylmethanol (50 mmol). The reaction mixture was then stirred at 65° C. overnight. Filtration and concentration gave a solid which was recrystallized to give the desired product as a white solid (9.5 g).

Aufarbeitung

  1. filtrationFiltration and concentration
  2. customgave a solid which
  3. customwas recrystallized

Quellen und Nachweise

ORD-Eintrag
ord-450c6013006144acab407f5f42709360
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08987284B2

Notizen zur Reaktion

Wird geladen…