HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491709Generated: October 25, 2026
Hydrochloric Acid → (1R)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethanol
https://huagongshe.com/reaction/1491709
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | [(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoate | HCID 10691998 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (1R)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethanol | HCID 10536015 | 98.5% |
Reaction Steps
[(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl] 3,5-dinitrobenzoate (50 g) was dissolved in methanol (2 liters). To the solution was added dropwise 1N sodium hydroxide aqueous solution (255 ml) at room temperature. The mixture was stirred for an hour at room temperature and neutralized with 1N hydrochloric acid (127 ml). Methanol was distilled off under reduced pressure. To the residue were added ethyl acetate (1liter) and water (200 ml). The mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline (200 ml), dried over magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1:3) to give (1R)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl] ethanol (25 g) as a pale yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371100 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-4dbea9fd49384f92855df76c4b98af8b |
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| Source note | uspto-grants-1994_12 |
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