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HRID 1033148作成日:2026年10月25日

3-Methyl-4-nitrobenzoic acid → alpha-[p-(dimethylamino)styryl]-N-(2-methyl-4-carboxyphenyl)nitrone

https://huagongshe.com/reaction/1033148

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-4-nitrobenzoic acidHCID 18370—
反応物4-(Dimethylamino)-cinnamaldehydeHCID 92224—
生成物alpha-[p-(dimethylamino)styryl]-N-(2-methyl-4-carboxyphenyl)nitroneHCID 8674782297.4%

反応手順

The general procedure of Example 1 was repeated except that 132.4 g (731 mmols) of 3 -methyl-4-nitrobenzoic acid was used instead of p-nitrobenzoic acid and 118.6 g (677 mmols) of 4-dimethylaminocinnamaldehyde was used instead of 4-diethylaminobenzaldehyde, thereby obtaining 213.8 g (yield 97.4%) of α-[p-(dimethylamino)styryl]-N-(2-methyl-4-carboxyphenyl)nitrone with a purity of 96%. The results of the analyses of the thus obtained compound are shown below.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05310620
出典データセットuspto-grants-1994_05
ORD IDord-f3fd399b812d4de2b4add459eb2b5145
出典メモuspto-grants-1994_05