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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419903Generated: November 1, 2026

HCID 70045808, compound → HCID 70048708, compound

https://huagongshe.com/reaction/1419903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70045808HCID 70045808—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 70048708HCID 7004870874%

Reaction Steps

Palladium on carbon (10%, 60 mg) was added to a solution of 4-benzyloxy-N-[2-[4-hydroxy-4-(4-methyl-benzyl)-piperidin-1-yl]-ethyl]-N-methyl-benzamide (226 mg, 0.48 mmol) in acetic acid (6 ml). The hydrogenation was complete after 4 h. The catalyst was removed by filtration through celite and the solvent was evaporated. Sodium bicarbonate (10% aq. solution, 2 ml) was added, and the aqeous layer extracted with dichloromethane. The organic layer was dried (Na2SO4), filtered and to give 4-hydroxy-N-[2-[4-hydroxy-4-(4-methyl-benzyl)-piperidin-1-yl]-ethyl ]-N-methyl-benzamide (135 mg, 74%) as a white solid. MS: me/e=383 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889026
Source datasetuspto-grants-1999_03
ORD IDord-18d262ffbad34368afc556b513a38b36
Source noteuspto-grants-1999_03