Reaktion #367490

ord-2b3502e5393e4644bdebfb3df05b7ba9

Reaktionsgleichung

Cc1ccc(CCN)cc1
2-(4-methylphenyl)ethanamine
O=CC(=O)c1cccc(C(F)(F)F)c1
3-trifluoromethylphenylglyoxal
O=CC(=O)c1ccccc1
phenylglyoxal
Cc1ccc(CCNCC(O)c2ccccc2)cc1
title compound
Cc1ccc(CCNCC(O)c2ccccc2)cc1
N-(2-(4-Methylphenyl)ethyl)-2-hydroxy-2-phenylethanamine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe title compound was prepared in the manner
  2. 2
    SonstigeThe chromatographed material was recrystallised from hexane

Vorschrift

The title compound was prepared in the manner described in Example 9, replacing 2-(4-methylphenyl)-1,1-dimethylethanamine by 2-(4-methylphenyl)ethanamine and 3-trifluoromethylphenylglyoxal by phenylglyoxal. The chromatographed material was recrystallised from hexane to give the title compound, mp 95°-97°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04588749uspto-grants-1986_05