Reacción #1350563

Ecuación de reacción

pyrrolidine

cyclooctanone

magnesium sulfate

→

desired product

N-cyclooctylpyrrolidine

Disolventes

hexane

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONflask was charged with 75 gm
2. 2
   Temperaturaheated
3. 3
   Temperaturaat reflux (the reaction
4. 4
   Otrofor 108 hours
5. 5
   FiltraciónThe reaction mixture was filtered through a fritted glass funnel
6. 6
   ConcentraciónThe filtrate was concentrated at reduced pressure on a rotary evaporator
7. 7
   Otroto give 70.5 gm

Procedimiento

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.

Fuente