Reacción #1970

Ecuación de reacción

4-t-butoxy-2,3,6-trifluoropyridine

LDA

hydrogen peroxide

sodium hydroxide

trimethoxyborane

→

title product

4-t-butoxy-2,3,6-trifluoro-5-hydroxypyridine

Disolventes

acetic acid

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGwith stirring for 25 min at -78° C
2. 2
   workup.STIRRINGthe mixture was stirred
3. 3
   Temperaturato warm to room temperature
4. 4
   Temperaturawhile cooling in an ice bath
5. 5
   workup.STIRRINGThe mixture was then stirred at room temperature for 16 hours
6. 6
   Otroquenched with saturated NH4Cl solution
7. 7
   ExtracciónThe mixture was extracted with ether
8. 8
   Lavadothe extract was washed with brine
9. 9
   Secadodried over MgSO4
10. 10
    OtroThe solvent was removed under vacuum
11. 11
    Otrothe residue was purified by flash chromatography on silica gel
12. 12
    Lavadoeluting with 1:8 ethyl acetate
13. 13
    OtroRemoval of the solvent

Procedimiento

A 11.16 g (54.39 mmol) sample of 4-t-butoxy-2,3,6-trifluoropyridine, from Example 253 step b above, was dissolved in 50 mL of THF, and the solution was cooled to -78° C. To this solution was added LDA (65.6 mmol) with stirring for 30 min, during which a solid preciptated. To this mixture was added 7.5 mL of trimethoxyborane, with stirring for 25 min at -78° C. To this mixture was added 10 mL of acetic acid, and the mixture was stirred and allowed to warm to room temperature. Next was added 100 mL of 30% hydrogen peroxide and 100 mL of 2N sodium hydroxide while cooling in an ice bath. The mixture was then stirred at room temperature for 16 hours, and quenched with saturated NH4Cl solution. The mixture was extracted with ether, and the extract was washed with brine and dried over MgSO4. The solvent was removed under vacuum, and the residue was purified by flash chromatography on silica gel, eluting with 1:8 ethyl acetate:hexane. Removal of the solvent gave 9.769 g of the title product as a colorless liquid.

Fuente