تفاعل #1973898

ord-69bb668264bc47cb9c49248df04e08dc

معادلة التفاعل

O=C1CCC2(CC1)OCCO2
1,4-dioxaspiro[4.5]decan-8-one
Cl
HCl
CCCCOc1cccc(F)c1F
3-Butoxy-1,2-difluorobenzene
[Li][CH2]CCC
n-Butyllithium
CCCCOc1ccc(C2(O)CCC3(CC2)OCCO3)c(F)c1F
8-(4-butoxy-2,3-difluorophenyl)-1,4-dioxaspiro[4.5]decan-8-ol
المردود 99.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added dropwise in the temperature range of −74° C. to −70° C.
  2. 2
    workup.WAITthe stirring was continued for another 8 hours while the mixture
  3. 3
    أخرىto come to 25° C
  4. 4
    أخرىThe resulting reaction mixture
  5. 5
    workup.ADDITIONmixed with them
  6. 6
    أخرىhad separated into organic and aqueous phases
  7. 7
    استخلاصthe extraction into an organic phase
  8. 8
    أخرىThe resulting organic phase was separated
  9. 9
    غسيلwashed successively with water
  10. 10
    تجفيفa saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate
  11. 11
    workup.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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08501038B2uspto-grants-2013_08