Reaktion #1172664

ord-69aef65087fc4fbb841f62084f0cb8ed

Reaktionsgleichung

c1ccc2c(c1)CC1OC21
1,2-Epoxy-2,3-dihydro-1-H indene
C1=Cc2ccccc2C1
indene
C1CCNC1
pyrrolidine
O[C@@H]1Cc2ccccc2[C@H]1N1CCCC1
trans-2,3-dihydro-2-hydroxy-1-(pyrrolidin-1-yl)-1H-indene

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeevaporated
  2. 2
    Sonstigeto remove the excess pyrrolidine under reduced pressure
  3. 3
    workup.DISTILLATIONThe residue was distilled under vacuum

Vorschrift

1,2-Epoxy-2,3-dihydro-1-H indene, prepared from indene (34.2 g) according to the procedure of M. Imuta and H. Ziffer, J. Org. Chem., 44, 1351 (1979), was treated immediately with pyrrolidine (50 ml). The exothermic reaction mixture was set aside for 15 minutes and then evaporated to remove the excess pyrrolidine under reduced pressure. The residue was distilled under vacuum to yield trans-2,3-dihydro-2-hydroxy-1-(pyrrolidin-1-yl)-1H-indene (10.2 g), b.p. 148°-150°/0.25 torr.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05010085uspto-grants-1991_04