Reaktion #354735

ord-57fe05309dae4472a9ac00f0582f7e80

Reaktionsgleichung

NCCc1c[nH]c2ccccc12
Tryptamine
CC(=O)CCC(=O)O
levulinic acid
CC12CCC(=O)N1CCc1c2[nH]c2ccccc12
title compound
CC12CCC(=O)N1CCc1c2[nH]c2ccccc12
1,2,5,6,11,11b-Hexahydro-11b-methyl-3H-indolizino[8,7-b]indol-3-one

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent is removed
  2. 2
    WaschenThe residue is successively washed with water, dilute aqueous sodium hydroxide, water, dilute aqueous hydrochloric acid, water
  3. 3
    Sonstigedried
  4. 4
    TrocknenTrituration of the crude product, decomposition at 252°-262°C., with methanol, and then with benzene, and drying
  5. 5
    Sonstigeprovides 120.4 g

Vorschrift

Tryptamine (112.15 g.), levulinic acid (97.6 g., 85.6 ml.) and butyl cellosolve (1 liter) are refluxed under nitrogen for 16 hours and the solvent is removed. The residue is successively washed with water, dilute aqueous sodium hydroxide, water, dilute aqueous hydrochloric acid, water and dried. Trituration of the crude product, decomposition at 252°-262°C., with methanol, and then with benzene, and drying provides 120.4 g. of the title compound, decomposition at 259°-263°C.; λmaxKBr 3.09, 6.01, 6.17, 13.38 μ.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03943148uspto-grants-1976_03