Reaktion #355278

ord-b46f88b6971443cb8f6bbd3404916606

Reaktionsgleichung

Cl
HCl
O=Cc1ccco1
Furfural
COc1ccc(N)cc1
p-anisidine
O=N[O-].[Na+]
sodium nitrite
COc1ccc(-c2ccc(C=O)o2)cc1
black semi-solid
Ausbeute 23.1%
COc1ccc(-c2ccc(C=O)o2)cc1
5-(4-Methoxyphenyl)-2-furaldehyde
Ausbeute 23.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethree-necked flask equipped with stirrer
  2. 2
    workup.ADDITIONwas introduced
  3. 3
    Temperaturmaintaining -10° to -5°C
  4. 4
    Extraktionthe reaction mixture was extracted with ether (1800 ml)
  5. 5
    TrocknenThe dried (MgSO4)
  6. 6
    Extraktionextract
  7. 7
    Sonstigewas evaporated in a rotary evaporator
  8. 8
    workup.DISTILLATIONthe residue was distilled under reduced pressure

Vorschrift

A 5l. three-necked flask equipped with stirrer, thermometer and dropping funnel was charged with water (150ml), concentrated HCl (400 ml) was introduced, followed by p-anisidine (185 g, 1.5 moles). A solution of sodium nitrite (108 g, 1.56 moles) in water (300 ml) was introduced dropwise maintaining -10° to -5°C. Furfural (184 g, 1.92 moles) was introduced followed by a solution of CuCl2.2H2O (46 g) in water (300 ml). The reaction mixture was heated to 53° with hot water maintaining 53°-68° for 2.5 hours. After cooling to room temperature overnight, the reaction mixture was extracted with ether (1800 ml). The dried (MgSO4) extract was evaporated in a rotary evaporator, and the residue was distilled under reduced pressure to give 70 g of black semi-solid product (b.p. 160°-190° at 2-5 mm).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03946049uspto-grants-1976_03