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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955237Generated: October 26, 2026

4-Benzylpiperidine → 4-Benzyl-1-(2-(4-benzyloxy-3-nitrophenoxy)ethyl)piperidine

https://huagongshe.com/reaction/1955237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzylpiperidineHCID 31738—
Reactant2-(4-Benzyloxy-3-nitrophenoxy)ethyl bromideHCID 23294404—
SolventTolueneHCID 1140—
Product4-Benzyl-1-(2-(4-benzyloxy-3-nitrophenoxy)ethyl)piperidineHCID 2329445277.1%

Reaction Steps

From a mixture of 4-benzylpiperidine (2.68 9, 15.1 mmol), 2-(4-benzyloxy-3-nitrophenoxy)ethyl bromide (2.65 g, 7.52 mmol) and KI (110 mg) in toluene (25 mL) was obtained 2.59 g (77%) of 4-benzyl-1-(2-(4-benzyloxy-3-nitrophenoxy)ethyl)piperidine as an orange-yellow oil. 1H NMR (CDCl3): 1.30-1.42 (m, 2H), 1.50-1.60 (m, 1H), 1.64-1.68 (m, 2H), 2.02-2.10 (m, 2H), 2.547 (d, 2H, J=7), 2.777 (t, 2H, T=6), 2.95-3.00 (m, 2H), 4.085 (t, 2H, J=6), 5.181 (s, 2H), 7.02-7.46 (m, 8H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124323
Source datasetuspto-grants-2000_09
ORD IDord-015a2e03db4545e89522ea4ccdaea661
Source noteuspto-grants-2000_09