Sodium Cyanide → 3-Fluoro-4-methoxyphenylacetonitrile

HRID 2050096

Reaktionsgleichung

Reaktionsgleichung von HRID 2050096
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][CH3:10])=[C:5]([F:11])[CH:4]=1.[CH2:12]([N:18](CCCCCC)CCCCCC)CCCCC.[C-]#N.[Na+]>O>[F:11][C:5]1[CH:4]=[C:3]([CH2:2][C:12]#[N:18])[CH:8]=[CH:7][C:6]=1[O:9][CH3:10]

Komponenten

5

Versuchsvorschrift

A mixture of 4-(bromomethyl)-2-fluoroanisole (45.8 g, 0.21 mol), trihexylamine (1.4 g) and sodium cyanide (20.5 g, 0.42 mol) in water (50 ml) is heated at 60°-65° C. for 18 hours. The mixture is cooled and extracted in its ether, washed with water, saturated sodium chloride solution and dried (CNa2SO4). Evaporation of the solvent gives a solid, (33.2 g): m.p. 42°-46° C.

Aufarbeitung

  1. temperatureis heated at 60°-65° C. for 18 hours
  2. temperatureThe mixture is cooled
  3. extractionextracted in its ether
  4. washwashed with water, saturated sodium chloride solution
  5. dry with materialdried (CNa2SO4)
  6. customEvaporation of the solvent
  7. customgives a solid, (33.2 g)

Quellen und Nachweise

ORD-Eintrag
ord-0b5c1373a8294b4196cf6dbc99e9e2f5
Quelldatensatz
uspto-grants-1980_04
Patentnummer
US04199595

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