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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264441Generated: October 30, 2026

Ozone → (RS)-2-(2-oxoethyl)-5,6-difluoro-1-indanone

https://huagongshe.com/reaction/264441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactant(RS)-2-(2-buten-1-yl)-5,6-difluoro-1-indanoneHCID 54100932—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(RS)-2-(2-oxoethyl)-5,6-difluoro-1-indanoneHCID 1903640876%

Reaction Steps

An ozone stream (2 g ozone/hour) was conducted for 40 minutes while stirring through a solution, cooled to -70°, of 5.3 g of (RS)-2-(2-buten-1-yl)-5,6-difluoro-1-indanone in 125 ml of anhydrous dichloromethane and 25 ml of anhydrous methanol. Subsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 2.64 ml of dimethyl sulfide, the mixture was stirred at room temperature for 16 hours. The reaction mixture was evaporated in a vacuum, the residue was treated with 60 ml of dichoromethane and, after the addition of 10 ml of water and 10 ml of trifluoroacetic acid, stirred at room temperature for 2 hours. The mixture was subsequently poured into 80 ml of water and neutralized by the spatula-wise addition of sodium hydrogen carbonate while stirring. An additional 40 ml of water were added, the phases were separated and the aqueous phase was extracted twice with 100 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. There was obtained a yellow oil which was crystallized from diethyl ether/hexane. 3.82 g (76%) of (RS)-2-(2-oxoethyl)-5,6-difluoro-1-indanone were obtained as a white solid with m.p. 78°-81°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-6bed122bb3864127a7ad2dea0819cdfc
Source noteuspto-grants-1997_07