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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653864Generated: October 31, 2026

Iodine → 1-(4-Iodophenyl)piperazine

https://huagongshe.com/reaction/1653864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant1-PhenylpiperazineHCID 7096—
CatalystSilver benzoateHCID 164649—
SolventAcetic AcidHCID 176—
Product1-(4-Iodophenyl)piperazineHCID 414784511.3%

Reaction Steps

Over a period of 15 minutes samples of iodine (8.62 grams, 0.034mol) and silver benzoate (7.78 grams, 0.034 mol) were added in portions to a magnetically stirred solution of 5 grams of 1-phenylpiperazine in 80 mL acetic acid. The mixture stirred for 1 hour. The solvent was evaporated and the residue partioned between 150 mL diethyl ether and 150 mL 2N sodium hydroxide. The organic layer was washed with 100 mL water, 100 mL brine, then dried over potassium carbonate and concentrated in vacuo to yield 1.0 gram (11%)of 1-(4-iodophenyl)-piperzine (110°-115° C.). The material obtained was used without further purification. 1H NMR (CDCl3, dTMS) 7.51 (2 H, d, 3JHH=9 Hz, m-ArH), 6.69 (2H, d, 3JHH=9 Hz, o-ArH), 3.17 (4H, m), 3.04 (4H, m). 13C NMR (CDCl3) 151.36, 137.73, 118.05, 81.35, 49.92, 45.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05403836
Source datasetuspto-grants-1995_04
ORD IDord-06234a554fe4473aab06933fc9afc7f3
Source noteuspto-grants-1995_04