반응 #932576

ord-4ea7f2738d8b42ddb07024ae3343deb5

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도To a stirred, cooled
  2. 2
    기타at 10°-25° C
  3. 3
    workup.ADDITIONWhen the addition
  4. 4
    기타the cooling bath was removed
  5. 5
    workup.ADDITIONThe reaction mixture was added portionwise
  6. 6
    workup.STIRRINGwith stirring to a cooled solution of 122 ml of 45% potassium hydroxide and 230 g of ice at a rate
  7. 7
    기타at 25°-35° C
  8. 8
    기타The reaction mixture was partitioned between ether and water
  9. 9
    건조The ether portion was dried
  10. 10
    농축concentrated in vacuo

실험 절차

To a stirred, cooled suspension of 34.7 g (0.167 ml) of phosphorous pentachloride in 20 ml of dry toluene (argon atmosphere) was added a solution of 31.93 g (0.159 m) of 1-[3-(1,1-dimethylethoxy)-2-hydroxypropyl]pyrrolidine (the product of Example 13a) and excess hydrogen chloride (gas) in 46 ml of dry toluene and 50 ml of dry tetrahydrofuran at a rate to keep the reaction temperature at 10°-25° C. When the addition was completed, the cooling bath was removed and the reaction mixture was stirred at ambient temperature for 1.5 hr. The reaction mixture was added portionwise, with stirring to a cooled solution of 122 ml of 45% potassium hydroxide and 230 g of ice at a rate to keep the reaction temperature at 25°-35° C. The reaction mixture was partitioned between ether and water. The ether portion was dried and concentrated in vacuo to give 31.69 g of oily title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04758563uspto-grants-1988_07