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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264503Generated: November 1, 2026

Ozone → HCID 19036568, compound

https://huagongshe.com/reaction/264503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantHCID 53807888HCID 53807888—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 19036568HCID 1903656873%

Reaction Steps

An ozone stream (1.5 g ozone/hour) was conducted for 60 minutes while stirring through a solution, cooled to -70°, of 8.1 g of (RS)-2-(2-buten-1-yl)-6-cyclopentoxy-1-indanone in 150 ml of anhydrous dichloromethane and 30 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 3.29 ml of dimethyl sulfide, the mixture was stirred at room temperature for 21 hours. The reaction mixture was evaporated in a vacuum. The residue was treated with 75 ml of dichoromethane and, after the addition of 12.5 ml of water and 12.5 ml of trifluoroacetic acid, stirred at room temperature for 5 hours. The mixture was subsequently poured into 150 ml of water and neutralized by the spatula-wise addition of sodium hydrogen carbonate while stirring. An additional 50 ml of water were added. The phases were separated and the aqueous phase was extracted twice with 150 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. 5.63 g (73%) of (RS)-2-(2-oxoethyl)-6-cyclopentoxy-1-indanone were obtained as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-fd69a075e7f04de89d26d490bc756259
Source noteuspto-grants-1997_07