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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087815Generated: October 26, 2026

N-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamide → N-[4-(1-Piperazinyl)phenyl]acetamide

https://huagongshe.com/reaction/1087815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-(4-(Phenylmethyl)-1-piperazinyl)phenyl)acetamideHCID 960610—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-[4-(1-Piperazinyl)phenyl]acetamideHCID 1563176156%

Reaction Steps

This compound was prepared by the hydrogenation of 7.7 (0.025 mole) of N-[4-[4-(phenylmethyl)-1-piperazinyl]phenyl]acetamide in 100 ml of methanol using palladium on carbon as the catalyst. The solution was filtered and the filtrate concentrated under reduced pressure to give an oil which crystallized. The solid was dissolved in a minimum amount of a methylene chloride/10% methanol solution and passed through a 100 g Florisil® column. The desired fractions were concentrated to an oil under reduced pressure which crystallized to give 3.1 g (56%) crude product. A 0.5 g portion was recrystallized from methanol/petroleum ether to give cream colored solid, m.p. 191°-193° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04960776
Source datasetuspto-grants-1990_10
ORD IDord-fea3129dcd2645d18642fb590b795be2
Source noteuspto-grants-1990_10