반응 #640601

ord-874bc4b2fca14bffad4e143260e7824a

반응 방정식

Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
CC(=O)N1CCC(=O)CC1
1-acetyl-4-piperidinone
C1CCNC1
pyrrolidine
Cc1ccccc1
toluene
CC(=O)N1CC=C(N2CCCC2)CC1
1-(4-pyrrolidin-1-yl-3,6-dihydro-2H-pyridin-1-yl)-ethanone

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타After removal of the solvent under a vacuum, 7.7 g (99% of theoretical) of the desired product 1-(4-pyrrolidin-1-yl-3,6-dihydro-2H-pyridin-1-yl)-ethanone (A)
  2. 2
    기타were obtained in the form of a brown-red oil

실험 절차

A mixture of 4.95 mL (40 mmol) of 1-acetyl-4-piperidinone, 3.64 mL (44 mmol) of pyrrolidine, 15 mL of toluene and a catalytic quantity of p-toluenesulfonic acid was heated for 12 h with refluxing on a water separator. After removal of the solvent under a vacuum, 7.7 g (99% of theoretical) of the desired product 1-(4-pyrrolidin-1-yl-3,6-dihydro-2H-pyridin-1-yl)-ethanone (A) were obtained in the form of a brown-red oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08048879B2uspto-grants-2011_11