تفاعل #77879

ord-104634446aeb42d7ba0c56844f5c4ea7

معادلة التفاعل

Cl
hydrochloric acid
O=C1CN2CCC1CC2
3-quinuclidinone
C=[CH][Mg][Br]
vinylmagnesium bromide
[Na+].[OH-]
sodium hydroxide
C=CC1(O)CN2CCC1CC2
title compound
المردود 54.0%
C=CC1(O)CN2CCC1CC2
3-Ethenyl-3-hydroxy-1-azabicyclo[2.2.2]octane
المردود 54.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled to 0° C.
  2. 2
    workup.STIRRINGThe mixture was stirred for 15 minutes
  3. 3
    استخلاصextracted with chloroform (4×50 mL) and chloroform/methanol (4:1, 50 mL)
  4. 4
    تجفيفdried (MgSO4)
  5. 5
    أخرىevaporated under reduced pressure
  6. 6
    أخرىpurified by flash chromatography (eluting with ammoniated chloroform/methanol, 85:15)

الإجراء التجريبي

Under an argon atmosphere, a solution of 3-quinuclidinone (1.25 g, 10 mmol) in anhydrous tetrahydrofuran (10 mL) was added over 15 minutes to a 1 M solution of vinylmagnesium bromide in tetrahydrofuran (20 mL, 20 mmol) at 0° C. to 5° C., stirred at room temperature for 24 hours, cooled to 0° C., and acidified to pH 1 with 6 M hydrochloric acid. The mixture was stirred for 15 minutes, basified to pH 10 with 25% aqueous sodium hydroxide, extracted with chloroform (4×50 mL) and chloroform/methanol (4:1, 50 mL), combined the organic layers, dried (MgSO4), evaporated under reduced pressure and purified by flash chromatography (eluting with ammoniated chloroform/methanol, 85:15) to obtain the title compound (830 mg, 5.4 mmol, 54%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06706878B2uspto-grants-2004_03