HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264488Generated: November 1, 2026
Ozone → (RS)-2-(2-oxoethyl)-6-tert-butyl-1-indanone
https://huagongshe.com/reaction/264488
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ozone | HCID 24823 | — |
| Reactant | (RS)-2-(2-buten-1-yl)-6-tert-butyl-1-indanone | HCID 53952129 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (RS)-2-(2-oxoethyl)-6-tert-butyl-1-indanone | HCID 19036442 | 92% |
Reaction Steps
An ozone stream (3 g ozone/hour) was conducted for 35 minutes while stirring through a solution, cooled to -70°, of 7.35 g of (RS)-2-(2-buten-1-yl)-6-tert-butyl-1-indanone in 150 ml of anhydrous dichloromethane and 30 ml of anhydrous methanol. Subsequently, the solution was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 3.36 ml of dimethyl sulfide, the mixture was stirred at room temperature for 17 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 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 50 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. 6.44 g (92%) of (RS)-2-(2-oxoethyl)-6-tert-butyl-1-indanone were obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646173 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-e128150ecf21427191a4bff074780c4c |
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| Source note | uspto-grants-1997_07 |
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