Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264519Generated: November 4, 2026

Ozone → (RS)-2-(2-oxoethyl)-4-methyl-1-indanone

https://huagongshe.com/reaction/264519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactant(RS)-2-(2-buten-1-yl)-4-methyl-1-indanoneHCID 54262890—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(RS)-2-(2-oxoethyl)-4-methyl-1-indanoneHCID 1903649194%

Reaction Steps

An ozone stream (3 g ozone/hour) was conducted for 90 minutes while stirring through a solution, cooled to -70°, of 12.0 g of (RS)-2-(2-buten-1-yl)-4-methyl-1-indanone in 220 ml of anhydrous dichloromethane and 45 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 6.6 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 160 ml of dichoromethane and, after the addition of 20 ml of water and 20 ml of trifluoroacetic acid, stirred at room temperature for 2 hours. The mixture was subsequently poured into 200 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. 10.6 g (94%) of (RS)-2-(2-oxoethyl)-4-methyl-1-indanone were obtained as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-b66ba437602a41948ba7491c91dedbc1
Source noteuspto-grants-1997_07