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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937149Generated: October 27, 2026

(2R,3S)-2-(4-Fluorophenyl)-3-methyl-2-(1H-1,2,4-triazol-1-yl)methyloxirane → HCID 178462387, compound

https://huagongshe.com/reaction/1937149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,3S)-2-(4-Fluorophenyl)-3-methyl-2-(1H-1,2,4-triazol-1-yl)methyloxiraneHCID 10443975—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178477152HCID 178477152—
SolventEthanolHCID 702—
ProductHCID 178462387HCID 17846238772.2%

Reaction Conditions

Temperature80 °C

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 descriptive 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06392082B1
Source datasetuspto-grants-2002_05
ORD IDord-a956192547b847c8b77dd1763e39769a
Source noteuspto-grants-2002_05