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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701853Generated: November 1, 2026

HCID 2827470, compound → 4-Amino-N-(1-phenylethyl)benzamide

https://huagongshe.com/reaction/1701853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2827470HCID 2827470—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Amino-N-(1-phenylethyl)benzamideHCID 126157—

Reaction Steps

A solution of 5 g (0.018 mole) of 4-nitro-N(alpha-methylbenzyl)-benzamide (#3) in 200-ml of absolute ethanol was added to a Paar hydrogenation bottle. To the solution was added a 0.4 g sample of 5% palladium on charcoal and the bottle placed on a Paar low-pressure hydrogenation apparatus. The mixture was shaken at room temperature in the presence of 45 p.s.i. of hydrogen for 2.5 hours. The catalyst was then removed by filtration through celite and the ethanol evaporated to yield the desired compound, 4-amino-N-(alpha-methylbenzyl)-benzamide (#4). Recrystallization from benzene produced the compound in pure form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379165
Source datasetuspto-grants-1983_04
ORD IDord-58bfede108ec42d39df52026ab205b00
Source noteuspto-grants-1983_04