HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 3-Ethyl-5-[2-(2,3-epoxypropoxy)-styryl]-isoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Epibromohydrin | HCID 18430 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 136136666 | HCID 136136666 | — |
| Product | 3-Ethyl-5-[2-(2,3-epoxypropoxy)-styryl]-isoxazole | HCID 54459660 | — |
Reaction Steps
This compound is prepared, using the method described in Example V, from 5.1 g of 55% strength sodium hydride (0.116 mole), 25.0 g (0.116 mole) of 3-ethyl-5-(2-hydroxystyryl)-isoxazole and 15.9 g (0.116 mole) of epibromohydrin. The reaction mixture is poured into sodium chloride solution and the batch is extracted by shaking with diethyl ether. The ether solution is dried with anhydrous sodium sulfate and evaporated down. 29.2 g (93% of theory) of a colorless oil are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04305951 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-434756edb36e4a2ea2f8dd8f7b8dfef8 |
| Source note | uspto-grants-1981_12 |