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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601682Generated: October 29, 2026

Acetonitrile → HCID 23158308, compound

https://huagongshe.com/reaction/601682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantNSC294179HCID 325437—
Reactant5-Bromo-1-indanoneHCID 520695—
ProductHCID 23158308HCID 23158308—

Reaction Steps

310 mg of [hydroxy (p-nitrobenzenesulfonyloxy]iodo]benzene was added at room temperature to 20 ml solution of acetonitrile with 130 mg of 5-bromo-1-indanone, and the mixture was heated under reflux for 3 hours. The reaction solution was cooled down to room temperature, the solvents were distilled outunder reduced pressure. The obtained residues were dissolved in 20 ml of ethanol, and refluxed all night. The reaction solution was cooled down to room temperature, the solvents were distilled outunder reduced pressure, dissolved in ethyl acetate, washed with water and saturated saline solution, and dried with anhydrous sodium sulfate. The residues obtained by distilling out the solvents under reduced pressure were purified by silicagel column chromatography (hexane:ethyl acetate=95:5) to obtain 84 mg of the above compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902369B2
Source datasetuspto-grants-2011_03
ORD IDord-6233cd6d7626445eb344e377d2ca1deb
Source noteuspto-grants-2011_03