HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496632Generated: October 31, 2026
Hydrogen Peroxide → 4-[2-Ethyl-4-(4-fluorophenyl)-1,3-thiazol-5-yl]pyridine 1-oxide
https://huagongshe.com/reaction/1496632
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | HCID 67436210 | HCID 67436210 | — |
| Catalyst | HCID 178477782 | HCID 178477782 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[2-Ethyl-4-(4-fluorophenyl)-1,3-thiazol-5-yl]pyridine 1-oxide | HCID 67537444 | 85% |
Reaction Steps
3.9 ml (44 mmol) of a 30% strength hydrogen peroxide solution are added dropwise with cooling to a solution of 2.18 g (7.24 mmol) of 4-[2-ethyl-4-(4-fluorophenyl)-1,3-thiazol-5-yl]pyridine and 46.2 mg (0.19 mmol) of methyltrioxorhenium (VII) in 10 ml dichloromethane such that the temperature of the reaction mixture does not exceed 15° C., and the mixture is stirred at room temperature for 16 h. The reaction mixture is then diluted with 100 ml of dichloromethane, and the organic phase is washed successively with 30 ml of a saturated aqueous NaHCO3 solution, 30 ml of a saturated Na2SO3 solution and 30 ml of water and dried over MgSO4. Under reduced pressure, the product is freed from the solvent, giving 1.98 g (85%) of the desired product; 1H-NMR(DMSO-d6) δ: 8.12 (d, 2H), 7.53 (m, 2H), 7.25 (d, 2H), 7.21 (m, 2H), 3.03 (q, 2H), 1.36 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09198426B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-0c546883ac6a4eeb9386a2bcfbc1e624 |
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| Source note | uspto-grants-2015_12 |
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