HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 1-(4-bromo-3-methylisoxazol-5-YL)cyclopropane-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67811851 | HCID 67811851 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-(4-bromo-3-methylisoxazol-5-YL)cyclopropane-1-carboxylate | HCID 67812454 | 94% |
Reaction Steps
To a solution of ethyl 1-(3-methylisoxazol-5-yl)cyclopropanecarboxylate (9.49 g, 48.6 mmol) in anhydrous DMF (50 mL) was added N-bromosuccinimide (10.31 g, 57.9 mmol). The reaction mixture was stirred at room temperature for 24 h. To the orange mixture was added water and the aqueous layer was extracted with MTBE (3×). The combined organic layers were washed with aqueous 10% sodium thiosulfate, water (2×) and dried to provide the product ethyl 1-(4-bromo-3-methylisoxazol-5-yl)cyclopropanecarboxylate (12.5 g, 45.6 mmol, 94% yield) as a light yellow oil. The product was used directly in the subsequent reaction without further purification. LC/MS m/z 274 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08796261B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-b36149b9077a4b9faa073851f64e1cbe |
| Source note | uspto-grants-2014_08 |