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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109839Generated: October 30, 2026

Ammonia → HCID 15219320, compound

https://huagongshe.com/reaction/1109839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 19708203HCID 19708203—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventIsopropanolHCID 3776—
ProductHCID 15219320HCID 1521932030%

Reaction Steps

To a sealed glass reaction vessel equipped with a thermometer, stirrer and reflux condenser, 10.7 g (0.02 mole) of 1,3-bis(3-nitro-4-bromobenzoyl)benzene, 0.43 g of a 5% palladium/activated carbon catalyst (a product of M. E. Chemcat Co.) and 50 ml of isopropyl alcohol were charged. Hydrogen was introduced with stirring at 30°~35° C. Absorbed hydrogen was 2.20 l (0.098 mole) over 9 hours. Successively, 3.6 g (0.06 mole) of a 28% aqueous ammonia solution was added and introduction of hydrogen was continued at 30°~35° C. for 6 hours and additionally at 60° C. for 4 hours with stirring. Further absorbed hydrogen was 0.401 g (0.018 mole). The catalyst was removed by filtration at the same temperature, 4.5 g of a 36% aqueous hydrochloric acid solution was added to the filtrate, and the mixture was allowed to cool. The precipitated crystal of 1,3-bis(3-aminobenzoyl)benzene hydrochloride were filtered, dissolved in 200 ml of water, and neutralized with a 28% aqueous ammonia solution. The precipitated crystals were filtered, washed and dried to obtain 1.9 g of 1,3-bis(3-aminobenzoyl)benzene. The yield was 30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05322962
Source datasetuspto-grants-1994_06
ORD IDord-13282579971b443f8ae4ebc5ecce84ad
Source noteuspto-grants-1994_06