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HRID 1243956作成日:2026年10月26日

Ammonia → Benzonitrile, 3-(aminomethyl)-

https://huagongshe.com/reaction/1243956

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物IsophthalonitrileHCID 12276—
反応物Sodium HydroxideHCID 14798—
反応物3-Cyanobenzoic acidHCID 15875—
反応物3-CyanobenzamideHCID 76974—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
生成物Benzonitrile, 3-(aminomethyl)-HCID 457594—

反応条件

温度50 °C

反応手順

A commercially available activated carbon-supported palladium catalyst “PDC-3000” available from Toyo C.C.I. Co., Ltd. (supported palladium: 3% by weight) was activated by reduction with hydrogen. A 100-ml autoclave was successively charged with 3.0 g of the activated catalyst, 12.8 g of isophthalonitrile containing as impurities 0.12% by weight of 3-cyanobenzamide and 0.12% by weight of 3-cyanobenzoic acid, 37 g of liquid ammonia, and 0.1 g of sodium hydroxide. Then, hydrogen was introduced into the autoclave to increase the inner pressure to 20 MPa (gauge). The concentration in the reaction solution was 0.043% by weight for the benzamide compound and 0.043% by weight for the benzoic acid compound. The autoclave was shaken at 50° C. for 30 min. The gas chromatographic analysis on the reaction product solution showed that the conversion of isophthalonitrile was 99.0 mol %, the yields of 3-cyanobenzylamine was 76.0 mol %, and the yield of m-xylylenediamine was 8.4 mol %. The by-products were substantially high-boiling substances.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07119230B2
出典データセットuspto-grants-2006_10
ORD IDord-465a8be7fc5940958d1aa44768404811
出典メモuspto-grants-2006_10