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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264482Generated: October 31, 2026

Ozone → HCID 19036558, compound

https://huagongshe.com/reaction/264482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantHCID 53994779HCID 53994779—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 19036558HCID 1903655895%

Reaction Steps

An ozone stream (2 g ozone/hour) was conducted for 50 minutes while stirring through a solution, cooled to -70°, of 5.6 g of (RS)-2-(2-buten-1-yl)-6-isopropyl-1-indanone in 125 ml of anhydrous dichloromethane and 25 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 2.7 ml of dimethyl sulfide, the mixture was stirred at room temperature for 15 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 3 hours. The mixture was subsequently poured into 50 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 200 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. 5.08 g (95%) of (RS)-2-(2-oxoethyl)-6-isopropyl-1-indanone were obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-ca51937cc6034738bac5ad846ee2086f
Source noteuspto-grants-1997_07