HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264374Generated: October 26, 2026
Ozone → (RS)-2-(2-oxoethyl)-6-chloro-1-indanone
https://huagongshe.com/reaction/264374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ozone | HCID 24823 | — |
| Reactant | (RS)-2-(2-buten-1-yl)-6-chloro-1-indanone | HCID 54260426 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (RS)-2-(2-oxoethyl)-6-chloro-1-indanone | HCID 10608460 | 85% |
Reaction Steps
An ozone stream (3 g ozone/hour) was conducted for 45 minutes while stirring through a solution, cooled to -70°, of 10.3 g of (RS)-2-(2-buten-1-yl)-6-chloro-1-indanone in 200 ml of anhydrous dichloro-methane and 100 ml of anhydrous methanol. Subsequently, the mixture was flushed with oxygen for 5 minutes and with argon for 10 minutes. After the addition of 5.13 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 60 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 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, concentrated in a vacuum and the crude product obtained was recrystallized from ethyl acetate/hexane. 8.29 g (85%) of (RS)-2-(2-oxoethyl)-6-chloro-1-indanone were obtained as a white solid with m.p. 80°.
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-592e41c62ee94dc6bd89b83bb370bd05 |
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| Source note | uspto-grants-1997_07 |
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