HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854167Generated: October 30, 2026
Potassium Carbonate → (R)-2-[2-(5-Fluoro-2-methylphenyl)-2-methylpropyl]-2-trifluoromethyloxirane
https://huagongshe.com/reaction/854167
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) | HCID 2735153 | — |
| Reactant | (S)-1,1,1-trifluoro-4-(5-fluoro-2-methylphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-ol | HCID 58933188 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-2-[2-(5-Fluoro-2-methylphenyl)-2-methylpropyl]-2-trifluoromethyloxirane | HCID 11701812 | 78% |
Reaction Steps
To a solution of (S)-1,1,1-trifluoro-4-(5-fluoro-2-methylphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-ol (1.37 g, 3.41 mmol) in 10 mL of anhydrous dichloromethane was added trimethyloxonium tetrafluoroborate (757 mg, 5.12 mmol). The resulting suspension was stirred at room temperature for 4.5 hours. A solution of potassium carbonate (1.41 g, 10.2 mmol) in 10 mL of water was then added. After 19 hours, the reaction mixture was poured into 40 mL of saturated aqueous sodium bicarbonate solution and extracted with three 50 mL portions of dichloromethane. The combined organic phases were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. Purification by column chromatography with silica gel (eluted with 0%-2% EtOAc-hexanes) afforded the title compound as a clear oil (731 mg, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256300B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-9b666b83b16d4b96b05a745eaec8e9af |
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| Source note | uspto-grants-2007_08 |
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