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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484498Generated: October 30, 2026

N-(2-hydroxyethyl)-4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzamide → N-(2-hydroxyethyl)-4-[(4-hydroxy-4-piperidinyl)methoxy]benzamide

https://huagongshe.com/reaction/484498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-hydroxyethyl)-4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzamideHCID 14989215—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-(2-hydroxyethyl)-4-[(4-hydroxy-4-piperidinyl)methoxy]benzamideHCID 1982092290.5%

Reaction Steps

A mixture of 23 parts of N-(2-hydroxyethyl)-4-[[4-hydroxy-1-(phenylmethyl)-4-piperidinyl]methoxy]benzamide and 200 parts of methanol was hydrogenated at normal pressure and at 50° C. with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated, yielding 16 parts (90.5%) of N-(2-hydroxyethyl)-4-[(4-hydroxy-4-piperidinyl) methoxy]benzamide as an oily residue (int. 81).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231184
Source datasetuspto-grants-1993_07
ORD IDord-db3aaf5907d049209f7c1c541887066c
Source noteuspto-grants-1993_07