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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291171Generated: October 30, 2026

HCID 18919836, compound → HCID 18919818, compound

https://huagongshe.com/reaction/1291171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18919836HCID 18919836—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 18919818HCID 1891981892.5%

Reaction Steps

0.48 g (0.00135 mol) of 1-(4-nitro-benzyl)-piperidin-4-yl 4-methyl-benzoate was dissolved in 27 ml of ethanol and treated with 0.48 g of Raney-nickel. The mixture was hydrogenated at room temperature and under normal pressure for 3 hrs. The catalyst was filtered off and, after concentration, the residue was chromatographed on silica gel with ethyl acetate/hexane (1:1→5:2) as the eluent. 0.405 g (92.5%) of 1-(4-amino-benzyl)-piperidin-4-yl 4-methyl-benzoate was obtained as a yellowish oil. MS: me/e=325 (C20H25N2O2+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-f6d7f92dcc2b4359ae2735facbc79540
Source noteuspto-grants-1998_05