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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264420Generated: November 1, 2026

Ozone → (RS)-2-(2-oxoethyl)-6-ethyl-indanone

https://huagongshe.com/reaction/264420

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactant(RS)-2-(2-buten-1-yl)-6-ethyl-1-indanoneHCID 54401231—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(RS)-2-(2-oxoethyl)-6-ethyl-indanoneHCID 1903652193%

Reaction Steps

An ozone stream (3 g ozone/hour) was conducted for 40 minutes while stirring through a solution, cooled to -70°, of 7.92 g of (RS)-2-(2-buten-1-yl)-6-ethyl-1-indanone in 150 ml of anhydrous dichloromethane and 30 ml of anhydrous methanol. Subsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 3.36 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 150 ml of dichoromethane and, after the addition of 30 ml of water and 30 ml of trifluoroacetic acid, stirred at room temperature for 3 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 100 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated in a vacuum. 6.94 g (93%) of (RS)-2-(2-oxoethyl)-6-ethyl-indanone were obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-e6ddfb640df64e44b2e22e9dd33d01fc
Source noteuspto-grants-1997_07