تفاعل #1350563

ord-83672f95bc0349c5924da434cd80475a

معادلة التفاعل

C1CCNC1
pyrrolidine
O=C1CCCCCCC1
cyclooctanone
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
C1CCCC(N2CCCC2)CCC1
desired product
C1CCCC(N2CCCC2)CCC1
N-cyclooctylpyrrolidine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONflask was charged with 75 gm
  2. 2
    درجة الحرارةheated
  3. 3
    درجة الحرارةat reflux (the reaction
  4. 4
    أخرىfor 108 hours
  5. 5
    ترشيحThe reaction mixture was filtered through a fritted glass funnel
  6. 6
    تركيزThe filtrate was concentrated at reduced pressure on a rotary evaporator
  7. 7
    أخرىto give 70.5 gm

الإجراء التجريبي

A three-neck 3000 ml. flask was charged with 75 gm. (1.05 moles) of pyrrolidine, 51 gm. cyclooctanone (0.4 mole) and 80 ml. anhydrous hexane. To the resulting solution, 80 gm. (0.8 mole) of anhydrous magnesium sulfate was added and the mixture was mechanically stirred and heated at reflux (the reaction was monitored by NMR analysis) for 108 hours. The reaction mixture was filtered through a fritted glass funnel. The filtrate was concentrated at reduced pressure on a rotary evaporator to give 70.5 gm. of a clear (yellow-tinted) oily substance. 1H-NMR and 13C-NMR spectra were acceptable for the desired product, 1-(1-pyrrolino)cyclooctene. Saturation of the 1-(1-pyrrolino)cyclooctene to give N-cyclooctylpyrrolidine was accomplished in 98% yield by catalytic hydrogenation in ethanol at a 55 psi pressure of hydrogen gas in the presence of 10% Pd on activated carbon.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06540905B1uspto-grants-2003_04