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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantIodine pentoxideHCID 159402—
Reactant(+,-) Trans-propane-2-sulfonic Acid (2-phenyl-cyclopentyl)-amideHCID 10956500—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetic AcidHCID 176—
Product(+,-) Trans Propane-2-sulfonic Acid [2-(4-iodo-phenyl)-cyclopentyl]-amideHCID 11784171187.5%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06639107B1
Source datasetuspto-grants-2003_10
ORD IDord-1340a906f63c415a8cfb501561f1444f
Source noteuspto-grants-2003_10