HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659886Generated: November 2, 2026
Sodium hydride → 3-Methyl-5-(2-hydroxy-styryl)-isoxazole
https://huagongshe.com/reaction/1659886
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Diethylphosphonomethyl-3-methylisoxazole | HCID 10585698 | — |
| Reactant | HCID 12520066 | HCID 12520066 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-Methyl-5-(2-hydroxy-styryl)-isoxazole | HCID 840164 | — |
Reaction Steps
8.8 g (0.2 mole) of a 55% strength suspension of sodium hydride in paraffin oil are introduced into 100 ml of absolute dimethylsulfoxide. 47 g (0.2 mole) of diethyl (3-methyl-isoxazol-5-yl)-methanephosphonate are added dropwise at room temperature. The mixture is then stirred for 30 minutes, after which 36 g (0.2 mole) of o-(1-methoxyethoxy)-benzaldehyde are added dropwise, with continued stirring. The reaction mixture is then stirred for 24 hours at room temperature and is poured onto 1 liter of ice water, and the batch is extracted 3 times with 80 ml of methylene chloride at a time. The combined organic phases are dried with sodium sulfate and evaporated down on a rotary evaporator. The oily residue is dissolved in 80 ml of methanol and 10 ml of water, 2 ml of 5 N HCl are added, and the mixture is stirred for 10 minutes. Excess water is then added slowly until a precipitate forms. This is filtered off, washed with water and recrystallized from ethanol. 19 g (47% of theory) of colorless crystals, of melting point 236°-238° C., are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04305951 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-569e88b4fd6b470c9ecb16d5fcb95107 |
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| Source note | uspto-grants-1981_12 |
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