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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765021Generated: October 28, 2026

Iodine → HCID 21106352, compound

https://huagongshe.com/reaction/1765021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant5-NitroindolineHCID 36219—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 21106352HCID 2110635298.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of silver sulfate (100 g, 0.32 mol) and iodine (82 g, 0.32 mol) in N,N-dimethylformamide (700 mL) and ethanol (1400 mL) was treated with 5-nitro-2,3-dihydro-1H-indole I (48 g, 0.29 mol). The resulting mixture was stirred at 25° C. for 1.5 h, filtered and the filter pad washed with ethyl acetate. The filtrate was concentrated in vacuo to a volume of approximately 500 mL. This solution was treated with a 1.0 N aqueous sodium thiosulfate solution (100 mL) and a saturated aqueous sodium chloride solution (400 mL). The resulting precipitate was collected by filtration, washed with water and petroleum ether, and dried in vacuo to afford 7-iodo-5-nitro-2,3-dihydro-1H-indole II (83.9 g, 98.9%) as a white solid: 1H NMR (DMSO-d6, 300 MHz) δ 8.18 (d, J=2.20 Hz, 1H), 7.80 (d, J=1.46 Hz, 1H), 7.03 (broad s, 1H), 3.65 (t, J=8.97 Hz, 2H), 3.17 (t, J=8.60 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226915B2
Source datasetuspto-grants-2007_06
ORD IDord-e4e2417bb23f474db60326e8d883e6c8
Source noteuspto-grants-2007_06