HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → HCID 70199106, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Nitrophthalic anhydride | HCID 21631 | — |
| Reactant | HCID 70200213 | HCID 70200213 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70199106 | HCID 70199106 | 42.3% |
Reaction Steps
A mixture of 7-amino-3-(1-hydroxy-l-methylethyl)-2-methylbenzo[b]furan (150 mg), 3-nitrophthalic anhydride (205 mg) and potassium carbonate (202 mg) in N,N-dimethylformamide (2 ml) was stirred at ambient temperature for 2 hours. Then, isopropyl iodide (280 mg) was added to the mixture and the mixture was stirred for 3 hours. The mixture was partitioned between ethyl acetate and brine. The organic layer was separated, dried over sodium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel and the obtained oil was crystallized from a mixture of 2-propanol and water to give 3-(1-hydroxy-1-methylethyl)-7-(6-isopropoxycarbonyl-2-nitrobenzoylamino)-2-methylbenzo[b]furan (136 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05858995 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ed249e175ffc45258f13bff5b820990c |
| Source note | uspto-grants-1999_01 |