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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366513Generated: October 29, 2026

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

https://huagongshe.com/reaction/366513

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 134-136βC; 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 numberUS06130234
Source datasetuspto-grants-2000_10
ORD IDord-b6daec08b6ec42b3888befbaaba3edfa
Source noteuspto-grants-2000_10