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HRID 280316作成日:2026年10月26日

2-(3-Chlorophenyl)-2-oxoacetaldehyde → N-(3-(4-Methylphenyl)-1,1-dimethylpropyl)-2-hydroxy-2-(3-chlorophenyl)ethanamine

https://huagongshe.com/reaction/280316

反応式

関与物質

役割名称HCID仕込み量
反応物2-(3-Chlorophenyl)-2-oxoacetaldehydeHCID 12463893—
反応物2-Methyl-4-(4-methylphenyl)butan-2-amineHCID 23322167—
生成物N-(3-(4-Methylphenyl)-1,1-dimethylpropyl)-2-hydroxy-2-(3-chlorophenyl)ethanamineHCID 23322177—

反応手順

The title compound was prepared in the manner described in Example 9 using 3-chlorophenylglyoxal and 3-(4-methylphenyl)-1,1-dimethylpropanamine. The chromatographed material was recrystallized from cyclohexane to give the title compound m.p. 136. τ(CDCL3 +d6DMSO) 8.9 (6H, s), 8.2-8.4 (2H, m), 7.7 (3H, s), 7.0-7.6 (4H, m), 5.35 (1H, dd), 2.9 (4H, s), 2.5-2.7 (5H, m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04588749
出典データセットuspto-grants-1986_05
ORD IDord-2d8e56e2bf444a0ab85fdddb57b92ca8
出典メモuspto-grants-1986_05