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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733113Generated: October 28, 2026

Acetonitrile → Ethanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-(2-naphthalenyl)-

https://huagongshe.com/reaction/733113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant2-AcetylnaphthaleneHCID 7122—
Reactant[Hydroxy(tosyloxy)iodo]benzeneHCID 325434—
SolventEthyl AcetateHCID 8857—
ProductEthanone, 2-[[(4-methylphenyl)sulfonyl]oxy]-1-(2-naphthalenyl)-HCID 1078334568.5%

Reaction Steps

Acetonitrile solution (40 mL) containing 2-acetonaphthone (1.70 g, 9.99 mmol) and [hydroxyl(tosyloxy)iodo]benzene (4.00 mg, 10.2 mmol) was heated under reflux for 3 hours. The reaction mixture was cooled, and ethyl acetate was added thereto. The reaction solution was washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous magnesium sulfate, and concentrated in vacuo to remove the solvent to obtain the title compound (2.33 g, 68.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589096B2
Source datasetuspto-grants-2009_09
ORD IDord-df93b800435f48b884e1d81f2190d520
Source noteuspto-grants-2009_09