Reacción #2028883

Ecuación de reacción

ethyl trifluoroacetate

1-tetralone

sodium methoxide

methanol

→

compound

Rendimiento 81.0%

2-trifluoroacetyl-1-tetralone

Rendimiento 81.0%

Disolventes

HCl

ether

ether

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.STIRRINGThe reaction mixture was stirred at room temperature for 14 hours
2. 2
   OtroThe phases were separated
3. 3
   Lavadothe organic layer was washed with 3N HCl
4. 4
   Secadowith brine, dried over anhydrous MgSO4
5. 5
   Filtraciónfiltered
6. 6
   Concentraciónconcentrated in vacuo
7. 7
   Otroformed which
8. 8
   Otrowere isolated by filtration and air
9. 9
   Otrodried

Procedimiento

A 250 mL one necked round bottom flask equipped with a reflux condenser, nitrogen inlet and provisions for magnetic stirring was charged with ethyl trifluoroacetate (28.4 g, 0.2 mol) and 75 mL of ether. To this solution was added 48 mL of 25% sodium methoxide in methanol (0.21 mol). A solution of 1-tetralone (29.2 g, 0.2 mol) in 50 mL of ether was added over about 5 minutes. The reaction mixture was stirred at room temperature for 14 hours and was diluted with 100 mL of 3N HCl. The phases were separated and the organic layer was washed with 3N HCl, and with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The residue was taken up in 70 mL of boiling ethanol/water and cooled to room temperature, whereupon crystals of 2-trifluoroacetyl-1-tetralone formed which were isolated by filtration and air dried to give pure compound (32 g, 81%): mp 48°-49° C.; 1H NMR CDCl3 δ 2.8 (m, 2H), 2.9 (m, 2H), 7.2 (d, j=3.0 Hz, 1H), 7.36 (m, 1H), 7.50 (m, 1H), 7.98 (m, 1H), 19F NMR CDCl3 δ −72.0. EI GC-MS M+=242.

Fuente