Reacción #2507822

Ecuación de reacción

p-toluenesulfonyl cyanide

n-butyl-lithium

7-bromo-6,6′-difluoro-3′-propyl-3,4,3′,4′-tetrahydro-2H,2′H-[3,7′]bichromenyl

→

6,6′-difluoro-3′-propyl-3,4,3′,4′-tetrahydro-2H,2′H-[3,7]bichromenyl-7-carbonitrile

Disolventes

ether

THF

hexane

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.WAITThe batch is left
2. 2
   Otrodoes not exceed −65° C
3. 3
   workup.WAITAfter 30 min
4. 4
   Lavadowashed with dil. hydrochloric acid
5. 5
   Secadophase is dried over sodium sulfate
6. 6
   Otroevaporated
7. 7
   Otrothe crude product is chromatographed on silica gel with heptane/toluene (2:3)

Procedimiento

1.4 g (3.31 mmol) of 7-bromo-6,6′-difluoro-3′-propyl-3,4,3′,4′-tetrahydro-2H,2′H-[3,7′]bichromenyl are dissolved in 20 ml of THF, and 3 ml (4.8 mmol) of a 15 percent solution of n-butyl-lithium in hexane are added at −50° C. The batch is left to stir for 2 h at −70° C., and a solution of 0.9 g (5.00 mmol) of p-toluenesulfonyl cyanide in 10 ml of THF is subsequently added at such a rate that the temperature does not exceed −65° C. After 30 min, the batch is allowed to thaw, diluted with ether and washed with dil. hydrochloric acid. The org. phase is dried over sodium sulfate and evaporated, and the crude product is chromatographed on silica gel with heptane/toluene (2:3), giving 6,6′-difluoro-3′-propyl-3,4,3′,4′-tetrahydro-2H,2′H-[3,7]bichromenyl-7-carbonitrile as colourless crystals of m.p. 122° C.

Fuente