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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291170Generated: November 2, 2026

HCID 18919752, compound → HCID 18919771, compound

https://huagongshe.com/reaction/1291170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18919752HCID 18919752—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 18919771HCID 1891977184.8%

Reaction Steps

0.13 g (0.00038 mol) of 1-(4-nitro-benzyl)-piperidin-4-yl benzoate was dissolved in 7.6 ml of ethanol and treated with 0.08 g of Raney-nickel. The mixture was hydrogenated at room temperature and under normal pressure for 2 hrs. The catalyst was filtered off and, after concentration, the residue was chromatographed on silica gel with ethyl acetate/hexane (1:1) as the eluent. 0.1 g (84%) of 1-(4-amino-benzyl)-piperidin-4-yl benzoate was obtained as a yellowish oil. MS: me/e=311 (C19H23N2 O2+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-2f379cd67486492e9412f17c802be644
Source noteuspto-grants-1998_05