반응 #1350563

ord-83672f95bc0349c5924da434cd80475a

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONflask was charged with 75 gm
  2. 2
    온도heated
  3. 3
    온도at reflux (the reaction
  4. 4
    기타for 108 hours
  5. 5
    여과The reaction mixture was filtered through a fritted glass funnel
  6. 6
    농축The filtrate was concentrated at reduced pressure on a rotary evaporator
  7. 7
    기타to give 70.5 gm

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06540905B1uspto-grants-2003_04