HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epibromohydrin → 3-Methyl-5-[2-(2,3-epoxypropoxy)-styryl]-isoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Methyl-5-(2-hydroxy-styryl)-isoxazole | HCID 840164 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-Methyl-5-[2-(2,3-epoxypropoxy)-styryl]-isoxazole | HCID 54495624 | — |
Reaction Steps
6.44 g of 55% strength sodium hydride in paraffin oil (0.15 mole) are introduced into 200 ml of absolute dimethylsulfoxide and 30 g (0.15 mole) of 3-methyl-5-(2-hydroxystyryl)-isoxazole, dissolved in 50 ml of dimethylsulfoxide, are added dropwise at room temperature. When the evolution of hydrogen has ceased, 20.2 g (0.15 mole) of epibromohydrin are added dropwise and the reaction mixture is stirred for 20 hours at room temperature. The mixture is then poured onto 1.5 liters of ice water and the solid precipitate is filtered off and recrystallized from isopropanol. 26.2 g (68% of theory) of colorless crystals, melting point 99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251539 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-80da21076aab482995194cc490b43895 |
| Source note | uspto-grants-1981_02 |