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HRID 885651作成日:2026年10月25日

Ethylenediamine → 2-Amino-5-cyano-N,3-dimethylbenzamide

https://huagongshe.com/reaction/885651

反応式

関与物質

役割名称HCID仕込み量
反応物EthylenediamineHCID 3301—
反応物MesityleneHCID 7947—
反応物Sodium CyanideHCID 8929—
反応物ButylimidazoleHCID 61347—
反応物2-amino-5-bromo-N,3-dimethylbenzamideHCID 44227575—
反応物NaOH NaClOHCID 86647248—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
生成物2-Amino-5-cyano-N,3-dimethylbenzamideHCID 25157282—

反応手順

A 500-mL four-necked flask equipped with a mechanical stirrer, thermocouple, condenser, side-arm addition funnel and sodium hydroxide/sodium hypochlorite scrubber was charged with 2-amino-5-bromo-N,3-dimethylbenzamide (prepared by the method of Reference Example 1) (24.6 g, 0.10 mol, 99% purity) and mesitylene (100 g) while maintaining an atmosphere of nitrogen through a gas inlet line connected to the condenser. The reaction mixture was stirred at room temperature and sodium cyanide (ground to a powder just prior to use) (6.2 g, 0.121 mol, assuming 95% purity), copper(I) iodide (2.9 g, 0.015 mol, 98% purity) and 1-butyl-1H-imidazole (10.8 g, 0.085 mol, 98% purity) were added, after which time the nitrogen inlet line was attached directly to the reaction flask. The reaction mixture was heated at reflux (about 166-170° C.) for 7 h, while venting through the scrubber. After cooling overnight, water (100 mL) was added to the reaction mixture and stirring was continued for 1 h. Ethylenediamine (0.09 g, about 0.015 mol, 99% purity) was added to the mixture, and stirring was continued for an additional 15 minutes. The mixture was filtered, and the solid collected was washed with water (3×50 mL), mesitylene (50 g) and dried to a constant weight in a vacuum-oven at 55° C. to give the title compound as a light brown solid (18.3 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242279B2
出典データセットuspto-grants-2012_08
ORD IDord-c1b2218dc90742a09db6f3360a0e31fb
出典メモuspto-grants-2012_08