Reaktion #367497

ord-2ffb7ddc52b84b30a66e254974a4796b

Reaktionsgleichung

O=CC(=O)c1ccccc1
phenylglyoxal
Cc1ccc(CC(C)(C)N)cc1
2-(4-methylphenyl)-1,1-dimethylethanamine
Cc1ccc(CC(C)(C)NCC(O)c2ccccc2)cc1
title compound
Cc1ccc(CC(C)(C)NCC(O)c2ccccc2)cc1
N-(2-(4-Methylphenyl)-1,1-dimethylethyl)-2-hydroxy-2-phenyl ethanamine

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 recrystallized from cyclohexane

Vorschrift

The title compound was prepared in the manner described in Example 9 using phenylglyoxal and 2-(4-methylphenyl)-1,1-dimethylethanamine. The chromatographed material was recrystallized from cyclohexane to give the title compound m.p. 137. τ(CDCl3 +d6DMSO) 8.95 (6H, s), 7.7 (3H, s), 7.35 (2H, s), 7.0-7.3 (2H, dd), 5.3 (1H, dd), 2.9 (4H, s), 2.5-2.7 (5H, m).

Quelle

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