Reacción #220442

Ecuación de reacción

HCl

tert-butyllithium

3-bromofluorobenzene

THF

anthranilonitrile

THF

→

2-Amino-3′-fluorobenzophenone

Disolventes

ethyl acetate

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrodid not rise above −74° C
2. 2
   TemperaturaThe reaction was warmed to 0° C.
3. 3
   workup.STIRRINGstirred for 2 hours
4. 4
   workup.STIRRINGstirring
5. 5
   workup.WAITcontinued for 30 minutes
6. 6
   Otrothe layers were separated
7. 7
   ExtracciónThe aqueous layer was back-extracted thrice with ethyl acetate
8. 8
   LavadoThe combined extracts were washed with brine
9. 9
   Secadodried over Na2SO4
10. 10
    Filtraciónfiltered
11. 11
    Concentraciónconcentrated
12. 12
    OtroThe residue was purified via HPLC
13. 13
    Lavadoeluting with 93:7 hexanes/ethyl acetate

Procedimiento

A solution of 3-bromofluorobenzene (1 eq.) in THF was cooled to −78° C. under nitrogen and treated with tert-butyllithium (2.05 eq., 1.6 M solution in pentane) at a rate of 40 ml/h. The internal temperature did not rise above −74° C. The orange solution was stirred at −78° C. for 30 minutes prior to the addition of anthranilonitrile (0.6 eq.) as a solution in THF. The reaction was warmed to 0° C. and stirred for 2 hours. 3N HCl was added to the mixture and stirring continued for 30 minutes. The reaction was diluted with ethyl acetate and the layers were separated. The aqueous layer was back-extracted thrice with ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified via HPLC eluting with 93:7 hexanes/ethyl acetate.

Fuente