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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100695Generated: November 2, 2026

Iodine → N-(5-iodo-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamide

https://huagongshe.com/reaction/2100695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantMetaperiodic acidHCID 65185—
ReactantN-(2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideHCID 46899808—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductN-(5-iodo-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideHCID 46899809483.7%

Reaction Steps

Intermediate 1 (1.75 g, 7.32 mmol) was dissolved in glacial acetic acid (30 ml) and then treated with concentrated sulfuric acid (0.8 ml) followed by water (2.8 ml) with stirring. This mixture was then treated with periodic acid (0.23 eq., 0.38 g, 1.67 mmol) then iodine (0.43 eq., 800 mg, 3.15 mmol), and the whole mix was stirred at 60° C. for 3-4 h. The reaction mixture was allowed to cool and then partitioned between ethyl acetate and 10% aqueous sodium metabisulfite. The organic layer was separated and dried over sodium sulphate and evaporated in vacuo to give the title compound as a yellow oil (2.95 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572819B2
Source datasetuspto-grants-2009_08
ORD IDord-0a0d98854a6b4a3dab1dbd92705fe28e
Source noteuspto-grants-2009_08