تفاعل #1973898
ord-69bb668264bc47cb9c49248df04e08dc
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwas added dropwise in the temperature range of −74° C. to −70° C.
- 2workup.WAITthe stirring was continued for another 8 hours while the mixture
- 3أخرىto come to 25° C
- 4أخرىThe resulting reaction mixture
- 5workup.ADDITIONmixed with them
- 6أخرىhad separated into organic and aqueous phases
- 7استخلاصthe extraction into an organic phase
- 8أخرىThe resulting organic phase was separated
- 9غسيلwashed successively with water
- 10تجفيفa saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate
- 11workup.DISTILLATIONThe solvent was then distilled off under reduced pressure
الإجراء التجريبي
3-Butoxy-1,2-difluorobenzene (7) (30.0 g) and THF (500 ml) were added to a reaction vessel under an atmosphere of nitrogen, and cooled to −74° C. n-Butyllithium (1.66 M in n-hexane solution; 120 ml) was added dropwise in the temperature range of −74° C. to −70° C. and the stirring was continued for another 2 hours. Successively, 1,4-dioxaspiro[4.5]decan-8-one (8) (30.2 g) in THF (200 ml) solution was added dropwise 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 resulting reaction mixture was poured into a 1N—HCl aqueous solution (500 ml) and ethyl acetate (500 ml) in a vessel and mixed with them. The mixture was then allowed to stand until it had separated into organic and aqueous phases, and the extraction into an organic phase was carried out. The resulting organic phase was separated, and washed successively with water, a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure to leave 8-(4-butoxy-2,3-difluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol (9) (55.0 g). The resulting compound (9) was a pale yellow oil.