Реакция #367500

Уравнение реакции

phenylglyoxal

2-(2,4-dimethylphenyl)-1-methylethanamine

→

title compound

N-(2-(2,4-Dimethylphenyl)-1-methylethyl)-2-hydroxy-2-phenyl ethanamine

Условия реакции

Обработка

1. 1
   ДругоеThe title compound was prepared in the manner
2. 2
   ДругоеThe residual oil was chromatographed on Kieselgel 60 using 3% methanol-chloroform
3. 3
   ДругоеRecrystallization of the resulting solid from hexane

Методика

The title compound was prepared in the manner described in Example 9 using phenylglyoxal and 2-(2,4-dimethylphenyl)-1-methylethanamine. The residual oil was chromatographed on Kieselgel 60 using 3% methanol-chloroform. Recrystallization of the resulting solid from hexane gave the title compound m.p. 91-92 as a 6:94 mixture of diastereoisomers. τ(CDCl3) 8.9 (3H, d, J=6 Hz), 7.7 (6H, s), 6.9-7.6 (5H, (m) +2H, disappears with D2O) 5.35 (1H, m), 3.05 (3H, s), 2.68 (5H, m).

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