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HRID 66704作成日:2026年10月27日

Ammonia → 2,4-Dimethylbenzene-1,3-diamine

https://huagongshe.com/reaction/66704

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物M-XyleneHCID 7929—
反応物IsophthalonitrileHCID 12276—
反応物HCID 178418361HCID 178418361—
溶媒Dicobalt Octacarbonyl (stabilized with 1-5% Hexane)HCID 25049—
生成物2,4-Dimethylbenzene-1,3-diamineHCID 4625581—

反応手順

0.76 g of dicobalt octacarbonyl, 0.3 g of various aromatic nitriles and 20 ml of m-xylene as a solvent were charged into a 100 ml eggplant type flask equipped with a reflux condenser and a gas inlet tube, and the air was thoroughly replaced while introducing nitrogen through the gas inlet tube. Thereafter, the flask was heated in an oil bath and the temperature of oil bath was elevated to 160° C. The flask was heated for 90 minutes under reflux conditions while passing nitrogen therethrough, and then the heating was discontinued and the flask was cooled to room temperature. The precipitate formed was directly transferred into a shaking type autoclave having a net capacity of 100 ml together with solvent m-xylene. After adding 10 g of isophthalonitrile and 10 ml of m-xylene thereto, the gas in the autoclave was replaced with nitrogen. After adding 10 ml of liquid ammonia thereto, hydrogen was fed up to a pressure of 260 kg/cm2 gage and the hydrogenation of isophthalonitrile was carried out at a reaction temperature of 100° C. until no absorption of hydrogen took place. The m-xylenediamine thus formed was analyzed by gas chromatography, the results as shown in Table 1 were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04343722
出典データセットuspto-grants-1982_08
ORD IDord-0236d8a247a7484099a69d9a281faa74
出典メモuspto-grants-1982_08