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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264363Generated: October 25, 2026

Ozone → (RS)-2-(2-oxoethyl)-3,3,6-trimethyl-1-indanone

https://huagongshe.com/reaction/264363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactant(RS)-2-(2-buten-1-yl)-3,3,6-trimethyl-1-indanoneHCID 53745382—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(RS)-2-(2-oxoethyl)-3,3,6-trimethyl-1-indanoneHCID 1063250894%

Reaction Steps

An ozone stream (2.5 g ozone/hour) was conducted for 60 minutes while stirring through a solution, cooled to -70° of 12.7 g (RS)-2-(2-buten-1-yl)-3,3,6-trimethyl-1-indanone in 200 ml of anhydrous dichloromethane and 40 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 6.12 ml of dimethyl sulfide, the mixture was stirred at room temperature for 18 hours. The reaction mixture was evaporated in a vacuum, the residue was treated with 150 ml of dichloromethane and, after the addition of 25 ml of water and 25 ml of trifluoroacetic acid, stirred at room temperature for 2.5 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 100 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. 11.3 g (94%) of (RS)-2-(2-oxoethyl)-3,3,6-trimethyl-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-1ae2dccc4c314ed1a20ba181c62f8de1
Source noteuspto-grants-1997_07