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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291165Generated: October 30, 2026

HCID 18919855, compound → HCID 18919852, compound

https://huagongshe.com/reaction/1291165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18919855HCID 18919855—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 18919852HCID 1891985252.1%

Reaction Steps

0.207 g (0.0006 mol) of 1-(3-nitro-benzyl)-piperidin-4-yl benzoate was dissolved in 12 ml of ethanol and treated with 0.12 g of Raney-nickel. The mixture was hydrogenated at room temperature and under normal pressure for 8 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. 0.097 g (52%) of 1-(3-amino-benzyl)-piperidin-4-yl benzoate was obtained as yellowish crystals; m.p. 95°-97°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-53f5df3fbe4945d28451aa189d0d9ef1
Source noteuspto-grants-1998_05