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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973791Generated: October 31, 2026

Ammonium Hydroxide → Phenylamino-1-(2-phenylethyl)-4-piperidinecarboxylic acid

https://huagongshe.com/reaction/1973791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantPhenylmethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylateHCID 12298150—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductPhenylamino-1-(2-phenylethyl)-4-piperidinecarboxylic acidHCID 86734310—

Reaction Steps

A mixture of 60 parts of phenylmethyl 4-(phenylamino)-1-(2-phenylethyl)-4-piperidinecarboxylate and 320 parts of methanol is hydrogenated at normal pressure and at room temperature with 10 parts of palladium-on-charcoal catalyst 10%. Upon the addition of a concentrated ammonium hydroxide solution, the precipitate, which is formed during the hydrogenation, is dissolved. The catalyst is filtered off and the filtrate is concentrated. Methanol is added and the whole is concentrated again. After cooling to room temperature the product is filtered off and dried in vacuo at 120° C, yielding 43.7 parts of 4-(phenylamino-1-(2-phenylethyl)-4-piperidinecarboxylic acid; mp. 268° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-c6692313b7da4e0aa778971ac01cf6cb
Source noteuspto-grants-1976_12