HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989486Generated: October 25, 2026
Iodine → (+,-) Trans Propane-2-sulfonic Acid [2-(4-iodo-phenyl)-cyclopentyl]-amide
https://huagongshe.com/reaction/989486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Iodine pentoxide | HCID 159402 | — |
| Reactant | (+,-) Trans-propane-2-sulfonic Acid (2-phenyl-cyclopentyl)-amide | HCID 10956500 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (+,-) Trans Propane-2-sulfonic Acid [2-(4-iodo-phenyl)-cyclopentyl]-amide | HCID 11784171 | 187.5% |
Reaction Steps
(+,−) Trans-propane-2-sulfonic acid (2-phenyl-cyclopentyl)-amide (0.52 g, 1.47 mmol, prepared in example 1) was dissolved in 30 mL of glacial acetic acid. To this solution was added concentrated sulfuric acid (0.16 mL, 1.61 mmol) at room temperature followed by iodine (0.19 g, 0.74 mmol), and diiodine pentoxide (0.20 g, 0.59 mmol). The reaction was then protected from light and heated to 90° C. and stirred for 22 hours. To the dark brown reaction mixture was slowly added 10% aqueous sodium bisulfite. The mixture was cooled to 0° C. for 1 hour and a light brown solid collected by filtration. The solid was dissolved in warm diethyl ether and washed with water (2×), then saturated sodium bicarbonate (1×). The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo to give 435 mg (75%) of the title compound. The NMR was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06639107B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-1340a906f63c415a8cfb501561f1444f |
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| Source note | uspto-grants-2003_10 |
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