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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66704Generated: October 25, 2026

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

https://huagongshe.com/reaction/66704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantM-XyleneHCID 7929—
ReactantIsophthalonitrileHCID 12276—
ReactantHCID 178418361HCID 178418361—
SolventDicobalt Octacarbonyl (stabilized with 1-5% Hexane)HCID 25049—
Product2,4-Dimethylbenzene-1,3-diamineHCID 4625581—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04343722
Source datasetuspto-grants-1982_08
ORD IDord-0236d8a247a7484099a69d9a281faa74
Source noteuspto-grants-1982_08