Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279371Generated: November 1, 2026

4-Iodoaniline → 1-(4-(4-Aminophenyl)-3-butynyl)-4-(4-chlorophenyl)-4-hydroxypiperidine

https://huagongshe.com/reaction/1279371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodoanilineHCID 10893—
Reactant1-(3-Butynyl)-4-(4-chlorophenyl)-4-hydroxypiperidineHCID 22225738—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventButylamineHCID 8007—
Product1-(4-(4-Aminophenyl)-3-butynyl)-4-(4-chlorophenyl)-4-hydroxypiperidineHCID 1842801121%

Reaction Steps

A solution of 1-(3-butynyl)-4-(4-chlorophenyl)-4-hydroxypiperidine (263 mg, 1.00 mmol), 4-iodoaniline (208 mg, 0.950 mmol) and 50 mg of tetrakis(triphenylphosphine) palladium in 10 mL of butylamine is allowed to reflux for 20 hr. The solvent is evaporated in vacuo to give a residue, which is purified by flash chromatography giving the product as an off white solid (70 mg, 21%): mp 134-136° C.; 1H NMR (CDCl3) 1.59 (m, 2 H), 1.90 (m, 2 H), 2.47 (m, 6 H), 2.67 (m, 2 H), 3.59 (S, 1 H), 3.87 (bs, 2 H), 6.46 (d, J=8.1 Hz, 1 H), 7.02 (d, J=8.1 Hz, 2 H), 7.14 (d, J=8.4 Hz, 2 H), 7.33 (d, J=8.4 Hz, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448270B1
Source datasetuspto-grants-2002_09
ORD IDord-a334544f251b4a4f9cb83c9a941d1b4c
Source noteuspto-grants-2002_09