Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279381Generated: November 1, 2026

4-Iodoaniline → 1-(4-(4-Aminophenyl)-3-butynyl)-4-(4-chlorobenzyl)piperidine

https://huagongshe.com/reaction/1279381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanilineHCID 10893—
Reactant4-(4-Chlorobenzyl)-1-(3-butynyl)piperidineHCID 10682872—
CatalystHCID 178418397HCID 178418397—
SolventButylamineHCID 8007—
Product1-(4-(4-Aminophenyl)-3-butynyl)-4-(4-chlorobenzyl)piperidineHCID 1061802512%

Reaction Steps

To a solution of 4-(4-chlorobenzyl)-1-(but-3-yn-1-yl)piperidine (318 mg, 1.21 mmol) and 4-iodoaniline (265 mg, 2.19 mmol) in 10 mL of butylamine is added 70 mg of Pd(PPh3)4. The resulting solution is allowed to reflux for 24 hr. The solvent is evaporated in vacuo and the residue is purified by flash chromatography giving the title product as a brown oil (50 mg, 12%): 1H NMR (CDCl3) 1.24 (m, 2 H), 1.44 (m, 1 H), 1.58 (m, 2 H), 1.96 ( m, 3 H), 2.15 (m, 2 H), 2.55 (m, 4 H), 2.89 (m, 2 H), 3.75 (bs, 2 H), 6.53 (d, J=6.0 Hz, 2 H), 7.05 (m, 2 H), 7.20 (m, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448270B1
Source datasetuspto-grants-2002_09
ORD IDord-53b0ceb41ec344188db13bb98c1b88a8
Source noteuspto-grants-2002_09