HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936844Generated: October 26, 2026
(2R,3S)-2-(4-Fluorophenyl)-3-methyl-2-(1H-1,2,4-triazol-1-yl)methyloxirane → HCID 178462387, compound
https://huagongshe.com/reaction/1936844
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2R,3S)-2-(4-Fluorophenyl)-3-methyl-2-(1H-1,2,4-triazol-1-yl)methyloxirane | HCID 10443975 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178477152 | HCID 178477152 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178462387 | HCID 178462387 | 72.2% |
Reaction Steps
1 ml (0.59 mmol) of a 4.8 M methanolic solution of sodium methoxide was added to a solution of 2.33 g (10 mmol) of (2R,3S)-2-(4-fluorophenyl)-3-methyl-2-[(1H-1,2,4-triazol-1-yl)methyl]oxirane [prepared as described in Chem. Pharm. Bull., 43, 441-449 (1995)] and 2.38 g (10 mmol) of cis-5-(acetylthio)-2-phenyl-1,3-dioxane [prepared as descripted in Step 6(i) above] in 40 ml of ethanol. The resulting mixture was stirred at 80° C. for 5 hours. After cooling, the reaction mixture was partitioned between ethyl acetate and water. The organic layer was separated and washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by chromatography on a silica gel (50 g) column using a 2:1 mixture of ethyl acetate and hexane as the eluant to afford 3.1 g (yield 72%) of the title compound as a brown foamy solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06391903B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-9988da6150244dbaa1e3e57f425bf59a |
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| Source note | uspto-grants-2002_05 |
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