HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537676Generated: October 30, 2026
2,4-Dichlorophenol → rac-(1S,5R)-3-[5-(2,4-dichlorophenoxy)-2-ethylphenyl]-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione
https://huagongshe.com/reaction/537676
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Dichlorophenol | HCID 8449 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 3-(5-Bromo-2-ethylphenyl)-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione | HCID 66679644 | — |
| Catalyst | copper(II) trifluoromethanesulfonate | HCID 2734996 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | rac-(1S,5R)-3-[5-(2,4-dichlorophenoxy)-2-ethylphenyl]-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione | HCID 66680478 | — |
Reaction Steps
To a mixture of rac-3-(5-bromo-2-ethylphenyl)-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione (0.175 g, 0.48 mmol), cesium carbonate (0.314 g, 0.96 mmol) and 2,4-dichlorophenol (0.393 g, 2.41 mmol) is added copper (II) trifluoromethanesulfonate (0.009 g, 0.024 mmol) and powdered 3 Å molecular sieves (0.200 g). Degassed anhydrous toluene (2 ml) is then added, followed by purging with nitrogen and heating at 170° C. for 1 hour under microwave irradiation. After cooling to room temperature the reaction mixture is quenched with 2M aqueous hydrochloric acid and extracted with dichloromethane (×2). The organic phase is separated and concentrated under reduced pressure. The crude product is then purified by preparative reverse phase HPLC to afford rac-(1S,5R)-3-[5-(2,4-dichlorophenoxy)-2-ethylphenyl]-1,8,8-trimethylbicyclo[3.2.1]octane-2,4-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865623B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-bc95a3534d304af7b9f4922945a75cf4 |
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| Source note | uspto-grants-2014_10 |
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