Реакция #367489

ord-250f6c9aa124474789d01ccb26ee94bd

Уравнение реакции

Cc1ccc(CCC(C)(C)N)cc1
3-(4-methylphenyl)-1,1-dimethylpropanamine
O=CC(=O)c1cccc(C(F)(F)F)c1
3-trifluoromethylphenyl glyoxal
O=CC(=O)c1ccccc1
phenylglyoxal
Cc1ccc(CCC(C)(C)NCC(O)c2ccccc2)cc1
title compound
Cc1ccc(CCC(C)(C)NCC(O)c2ccccc2)cc1
N-(3-(4-Methylphenyl)-1,1-dimethylpropyl)-2-hydroxy-2-phenyl ethanamine

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

The title compound was prepared in the manner described in Example 9, replacing 2-(4-methylphenyl)-1,1-dimethylethanamine by 3-(4-methylphenyl)-1,1-dimethylpropanamine and 3-trifluoromethylphenyl glyoxal by phenylglyoxal. The chromatographed material was recrystallised from hexane to give the title compound m.p. 107-110. τ (CDCl3) 8.95 (6H, s), 8.2-8.7 (2H, m), 7.8 (3H, s), 7.3-7.7 (4H, m), 5.7-6.5 (2H, m), 5.5 (1H, t, J=6 Hz), 2.9 (4H, s), 2.7 (4H, m).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04588749uspto-grants-1986_05