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HRID 40447作成日:2026年10月23日

4-(Dimethylamino)Benzaldehyde → n-(5-Carboxypentyl)-4-(4-(dimethylamino)styryl)pyridinium bromide

https://huagongshe.com/ja/reaction/40447

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Dimethylamino)BenzaldehydeHCID 7479—
反応物PiperidineHCID 8082—
反応物1-(5-Carboxy-pentyl)-2-methyl-pyridinium bromideHCID 66643503—
溶媒EthanolHCID 702—
生成物n-(5-Carboxypentyl)-4-(4-(dimethylamino)styryl)pyridinium bromideHCID 66643380—

反応条件

温度60 °C

反応手順

A mixture of 4-N,N-dimethylaminobenzaldehyde (3 g, 20 mmoles), N-(5-carboxy-pentyl)picolinium bromide (5.6 g, 20 mmoles) and piperidine (2 mL) in ethanol (100 mL) was heated at 60° C. overnight. The mixture was evaporated to dryness in vacuo. The residue was redissolved in methanol and then precipitated with ether to give the product (6.7 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530195B2
出典データセットuspto-grants-2013_09
ORD IDord-af6963a81e4745939b0548827d31456a
出典メモuspto-grants-2013_09