Reacción #2175430

Ecuación de reacción

1,4-dioxaspiro[4.5]decan-8-one

sec-Butyllithium

ammonium chloride

4′-Ethoxy-2,2′,3,3′-tetrafluoro-1,1′-biphenyl

→

8-(4′-ethoxy-2,2′,3,3′-tetrafluoro-1,1′-biphenyl-4-yl)-1,4-dioxaspiro[4.5]decan-8-ol

Disolventes

THF

n-hexane

cyclohexane

ethyl acetate

THF

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITION222 ml) was added dropwide
2. 2
   workup.ADDITIONwas added dropwise
3. 3
   workup.WAITin the temperature range of −75° C. to −70° C., and the stirring was continued for another 8 hours while the mixture
4. 4
   Otroto come to 25° C
5. 5
   workup.ADDITIONThe reaction mixture was poured into a vessel
6. 6
   workup.ADDITIONmixed with them
7. 7
   Otrohad separated into organic and aqueous phases
8. 8
   Extracciónthe extraction
9. 9
   LavadoThe combined organic phase was washed successively with water
10. 10
    Secadoa saturated aqueous solution of sodium hydrogencarbonate and water, and dried over anhydrous magnesium sulfate
11. 11
    workup.DISTILLATIONThen, the solvent was distilled off

Procedimiento

4′-Ethoxy-2,2′,3,3′-tetrafluoro-1,1′-biphenyl (s-25) (50 g) and THF (500 ml) were put in a reaction vessel under an atmosphere of nitrogen and cooled to −74° C. sec-Butyllithium (a 1.00 M solution in n-hexane and cyclohexane; 222 ml) was added dropwide thereto in the temperature range of −74° C. to −70° C., and the stirring was continued for another 2 hours. Then, 1,4-dioxaspiro[4.5]decan-8-one (s-12) (28.8 g) dissolved in THF (200 ml) was added dropwise thereto in the temperature range of −75° C. to −70° C., and the stirring was continued for another 8 hours while the mixture was allowed to come to 25° C. The reaction mixture was poured into a vessel containing an aqueous solution of ammonium chloride (3%; 500 ml) and ethyl acetate (500 ml), and mixed with them. The mixture was then allowed to stand until it had separated into organic and aqueous phases, and the extraction was carried out. The combined organic phase was washed successively with water, a saturated aqueous solution of sodium hydrogencarbonate and water, and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off to give 8-(4′-ethoxy-2,2′,3,3′-tetrafluoro-1,1′-biphenyl-4-yl)-1,4-dioxaspiro[4.5]decan-8-ol. p-Toluenesulfonic acid (1.5 g) and toluene (300 ml) were added to the compound and the mixture was heated to reflux for 2 hours, while distilled water was removed. After the reaction mixture had been cooled to 30° C., water (300 ml) and toluene (300 ml) were added to the mixture, and mixed with it. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases, and the extraction was carried out. The combined organic phase was washed successively with a saturated aqueous solution of sodium hydrogencarbonate and water, and dried over anhydrous magnesium sulfate. The resulting solution was purified by column chromatography using silica gel as a stationary phase powder and toluene as an eluent. The product was dissolved in a mixed solvent of toluene (100 ml) and Solmix A-11 100 ml), Pd/C (2.5 g) was added thereto, and the mixture was stirred at room temperature under an atmosphere of hydrogen until hydrogen absorption had ceased. After the completion of the reaction, Pd/C was removed and the solvent was distilled off. The resulting residue was purified by column chromatography using silica gel as a stationary phase powder and toluene as an eluent, and then by recrystallization from Solmix A-11 to give 8-(4′-ethoxy-2,2′,3,3′-tetrafluoro-1,1′-biphenyl-4-yl)-1,4-dioxaspiro[4.5]decane (s-26) (31.9 g). The yield based on the compound (s-25) was 42.0%.

Fuente