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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264413Generated: October 29, 2026

Ozone → 2-(6-ethoxy-1-oxo-2,3-dihydro-1H-inden-2-yl)acetaldehyde

https://huagongshe.com/reaction/264413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
Reactant(RS)-2-(2-buten-1-yl)-6-ethoxy-1-indanoneHCID 53729864—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-(6-ethoxy-1-oxo-2,3-dihydro-1H-inden-2-yl)acetaldehydeHCID 1903635764%

Reaction Steps

An ozone stream (3 g ozone/hour) was conducted for 90 minutes while stirring through a solution, cooled to -70°, of 5.6 g of (RS)-2-(2-buten-1-yl)-6-ethoxy-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 2.72 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 170 ml of dichoromethane and, after the addition of 25 ml of water and 25 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. 3.4 g (64%) of (RS)-2-(2-oxoethyl)-6-ethoxy-1-indanone were obtained as a red-brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646173
Source datasetuspto-grants-1997_07
ORD IDord-7e64b6789e9c4e1db93093096778f586
Source noteuspto-grants-1997_07