HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Bromo-4-nitrobenzene | HCID 11466 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | m-Chlorophenylacetonitrile | HCID 73722 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazole | HCID 12016670 | 34.8% |
Reaction Steps
Sodium hydroxide (0.62 mol) was dissolved in methanol (100 mol) and the mixture was cooled till room temperature. 1-bromo-4-nitro-benzene (0.124 mol), followed by 3-chloro-benzeneacetonitrile (0.223 mol) were added dropwise, the temperature raised till 50° C. and the mixture was stirred at room temperature for one night. The mixture was poured into water and ice, the precipitate was filtered off, washed with water and extracted with DME and methanol. The organic layer was dried (MgSO4), filtered off and evaporated till dryness. The residue was taken up in diethylether, filtered off and dried, yielding 13.2 g (34.8%) of 5-bromo-3-(3-chlorophenyl)-2,1-benzisoxazole, mp. 163° C. (intermediate 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067531B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-d43f8168d14e4e5a9ea48f992ca7aae4 |
| Source note | uspto-grants-2006_06 |