HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 3,6-Bis-allyloxy-5-nitrobenzo[d]isoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178526404 | HCID 178526404 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,6-Bis-allyloxy-5-nitrobenzo[d]isoxazole | HCID 66750987 | — |
Reaction Steps
To a suspension of 5-nitrobenzo[d]isoxazole-3,6-diol (1.1 g, 5.61 mmol) and potassium carbonate (3.9 g, 28.2 mmol) in DMF (10 mL) is added dropwise allyl bromide (1.42 mL, 8.30 mmol). The mixture is stirred at room temperature for 18 h. The mixture is diluted with EtOAc, and ice and water are added. The organic phase is separated and washed with water and brine, and dried over MgSO4, filtered and concentrated to afford 3,6-bis-allyloxy-5-nitrobenzo[d]isoxazole as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700633B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-2c906fd46f1a49499d32b446c10ea8d7 |
| Source note | uspto-grants-2010_04 |