HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854164Generated: November 2, 2026
Potassium Carbonate → (R)-2-[2-(5-Fluoro-2-methoxyphenyl)-2-methylpropyl]-2-trifluoromethyloxirane
https://huagongshe.com/reaction/854164
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-methoxyphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-ol | HCID 16115564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-2-[2-(5-Fluoro-2-methoxyphenyl)-2-methylpropyl]-2-trifluoromethyloxirane | HCID 11208565 | 95% |
Reaction Steps
To a solution of (S)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-p-tolylsulfanylmethylpentan-2-ol (42.7 g, 102 mmol) in 250 mL of anhydrous dichloromethane was added trimethyloxonium tetrafluoroborate (22.7 g, 153 mmol). The resulting suspension was stirred at room temperature for 4.5 hours. A solution of potassium carbonate (42.4 g, 307 mmol) in 250 mL of water was then added. After 16 hours, the reaction mixture was poured into 200 mL of saturated aqueous sodium bicarbonate solution and extracted with three 400 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 pale yellow oil (28.3 g, 95%).
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-7745338889884fc8ae96258e3775bef4 |
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| Source note | uspto-grants-2007_08 |
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