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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 5-(4-Methylpiperazin-1-yl)-2-trifluoromethoxyphenylamine | HCID 24994142 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[3-Iodo-4-(trifluoromethoxy)phenyl]-4-methylpiperazine | HCID 68728991 | 34.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426417B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-57d2814d96a74ad68e14ddae7f4a70a0 |
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| Source note | uspto-grants-2013_04 |
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