Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968558Generated: October 29, 2026

Hydrogen iodide → 1-[3-Iodo-4-(trifluoromethoxy)phenyl]-4-methylpiperazine

https://huagongshe.com/reaction/1968558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen iodideHCID 24841—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant5-(4-Methylpiperazin-1-yl)-2-trifluoromethoxyphenylamineHCID 24994142—
SolventDimethyl SulfoxideHCID 679—
Product1-[3-Iodo-4-(trifluoromethoxy)phenyl]-4-methylpiperazineHCID 6872899134.5%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of 2-trifluoromethoxy-5-(4-methyl-piperazin-1-yl)-phenylamine (5.0 g, 0.018 mol), sodium nitrite (5.1 g, 0.0734 mol) in dimethyl sulfoxide (180 mL) a solution of 57% hydroiodic acid (9.6. mL, 0.0427 mol) in dimethyl sulfoxide were added dropwise at room temperature in 20 minutes. The reaction was stirred for 5 hours at 35° C., then cooled in a ice bath and sodium bicarbonate in small portion was added until basic pH. The aqueous layer was extracted with dichoromethane (3×500 mL), the organic phases washed with 10% solution of sodium bisulphite (2×500 mL) then water (1×300 mL). The organic phase was dried over anhydrous Na2SO4, the solvent evaporated under vacuum to yield the intermediate (2.4 g, 34%) as a orange solid which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426417B2
Source datasetuspto-grants-2013_04
ORD IDord-57d2814d96a74ad68e14ddae7f4a70a0
Source noteuspto-grants-2013_04