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HRID 746149作成日:2026年10月26日

5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride → 1-[5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamido]pyridinium chloride

https://huagongshe.com/reaction/746149

反応式

関与物質

役割名称HCID仕込み量
反応物5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chlorideHCID 3017765—
反応物HCID 12210597HCID 12210597—
溶媒AcetonitrileHCID 6342—
生成物1-[5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamido]pyridinium chlorideHCID 20240778156.1%

反応手順

1-Aminopyridinium chloride (2.9 g) was added to 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoyl chloride (7.6 g) in acetonitrile (50 ml). The mixture was stirred and heated to reflux. After 20 minutes a solid precipitated. Reflux was continued for a further 40 minutes. Then the mixture was cooled in ice and the solid filtered off. The solid was washed with cold acetonitrile, then with ether, and was air dried to give 7.4 g of the desired product, mp 234°-237° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04602944
出典データセットuspto-grants-1986_07
ORD IDord-4593eaa837e64527a44451757e68ee7b
出典メモuspto-grants-1986_07