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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952987Generated: November 1, 2026

Ammonia → HCID 15480552, compound

https://huagongshe.com/reaction/1952987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPotassium BromideHCID 253877—
Reactant2-(4-Cyanophenyl)acetamideHCID 15480551—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
ProductHCID 15480552HCID 15480552—

Reaction Steps

0.65 g (4.057 mMol) of 4-cyanophenylacetamide were dissolved in 50 ml of methanol which was saturated with ammonia at+10° C. After the addition of 0.3 g of Raney nickel the mixture was hydrogenated in an autoclave at 40° C. under 5 bar of hydrogen pressure. After the uptake of hydrogen had ended the catalyst was filtered off and excess ammonia was distilled off with the solvent. The residue was acidified with 20 percent hydrochloric acid against Congo red and the non-basic impurities were removed by etherification. The ether extract was discarded, the aqueous solution was made alkaline with sodium hydroxide with external cooling and exhaustively extracted with ether. The ether solution was dried over caustic potash and freed from solvent, the residue was triturated with a few drops of ether and suction filtered. 610 mg (100% of theory) of colourless crystals were obtained, Mp. 138-140° C. IR (KBr): 1660.6, 1637.5 (Amide-C=O) cm-1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114390
Source datasetuspto-grants-2000_09
ORD IDord-67c18158ef3f425c872f24016fcb2868
Source noteuspto-grants-2000_09