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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291110Generated: October 30, 2026

HCID 18919793, compound → HCID 18919759, compound

https://huagongshe.com/reaction/1291110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18919793HCID 18919793—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 18919759HCID 1891975948%

Reaction Steps

0.25 g (0.000612 mol) of 1-benzyl-piperidin-4-yl 2-nitro-4-trifluoromethyl-benzoate was dissolved in 10 ml of ethanol and treated with 0.15 g of Raney-nickel. The mixture was hydrogenated at room temperature under normal pressure for 2 hrs. The catalyst was filtered off and the solvent was removed completely. The residue was chromatographed over silica gel with ethyl acetate/hexane (1:1) as the eluent. 0.11 g (48%) of 1-benzyl-piperidin-4-yl 2-amino-4-trifluoromethyl-benzoate was obtained as a yellow oil. MS: me/e=379 (C20H22F3N2 O2 +).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753679
Source datasetuspto-grants-1998_05
ORD IDord-9f0de566935c464695a3f1965bfc71a3
Source noteuspto-grants-1998_05