Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264385Generated: October 29, 2026

Ozone → HCID 19036450, compound

https://huagongshe.com/reaction/264385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantHCID 53950047HCID 53950047—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 19036450HCID 1903645097%

Reaction Steps

An ozone stream (3 g ozone/hour) was conducted for 40 minutes while stirring through a solution, cooled to -70°, of 8.2 g of (RS)-2-(2-buten-1-yl)-6-ethyl-3,3-dimethyl-1-indanone in 120 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 3.72 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 100 ml of dichoromethane and, after the addition of 15 ml of water and 15 ml of trifluoroacetic acid, stirred at room temperature for 2 hours. The mixture was subsequently poured into 100 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. 7.55 g (97%) of (RS)-2-(2-oxoethyl)-6-ethyl-3,3-dimethyl1-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-9d9b87f2f27f448885859d6df7cd77b5
Source noteuspto-grants-1997_07