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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264561Generated: November 1, 2026

Ozone → (RS)-2-(2-oxoethyl)-7-methoxy-1-indanone

https://huagongshe.com/reaction/264561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant(RS)-2-(2-buten-1-yl)-7-methoxy-1-indanoneHCID 53703468—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product(RS)-2-(2-oxoethyl)-7-methoxy-1-indanoneHCID 1051237771%

Reaction Steps

An ozone stream (3 g ozone/hour) was conducted while stirring for 45 minutes through a solution, cooled to -70°, of 9.9 g of (RS)-2-(2-buten-1-yl)-7-methoxy-1-indanone in 200 ml of anhydrous dichloromethane and 100 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 5 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 200 ml of dichloromethane and, after the addition of 20 ml of water and 20 ml of trifluoroacetic acid, stirred at room temperature for 3 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 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, concentrated in a vacuum and the crude product obtained was cystallized from ethyl acetate/hexane. 6.6 g (71%) of (RS)-2-(2-oxoethyl)-7-methoxy-1-indanone were obtained as a white solid with m.p. 102°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-07a6bf25767d4b3088c80c16cdae4c1a
Source noteuspto-grants-1997_07