Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium hydrogen persulfate | HCID 23690007 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 54299138 | HCID 54299138 | — |
| Product | HCID 13754490 | HCID 13754490 | — |
Reaction Steps
To a solution of 5.90 g (14.2 mmol) of 5-(1-methylethyl)-4-(4-methylthiophenyl)-α,α-bis(trifluoromethyl)thiazole-2-methanol in 200 ml of methanol at 25° C. was added 21.3 g (34.7 mmol) of Oxone® (potassium hydrogen persulfate) and the resulting suspension was stirred at 25° C. for 3 hours. The suspension was filtered, and the filtrate concentrated in vacuo. The residue was dissolved in ethyl acetate; and the solution was washed with distilled water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The crude product was recrystallized from n-butyl chloride to provide 3.34 g of 5-(1-methylethyl)-4-(4-methylsulfonylphenyl)-α,α-bis(trifluoromethyl)thiazole-2-methanol as a yellow crystalline solid, m.p. 122°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04632930 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-9ac9cdc2f09044ae94a3e9ff7051824c |
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| Source note | uspto-grants-1986_12 |
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