HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-methyl-N-methyloxy-2-benzyloxycarbonylamino-5-isobutyloxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-N-methyloxy-2-benzyloxycarbonylamino-5-hydroxybenzamide | HCID 18315375 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-methyl-N-methyloxy-2-benzyloxycarbonylamino-5-isobutyloxybenzamide | HCID 18315337 | — |
Reaction Steps
A solution of N-methyl-N-methyloxy-2-benzyloxycarbonylamino-5-hydroxybenzamide (3.0 g), isopropyl iodide (2.2 g) and potassium carbonate (2.0 g) in N,N-dimethylformamide (20 ml) was stirred for 15 hours at 70° C. To the reaction mixture was added water, which was subjected to extraction with ethyl acetate (80 ml). The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by means of a silica gel column chromatography to give N-methyl-N-methyloxy-2-benzyloxycarbonylamino-5-isobutyloxybenzamide.as an orange oily product (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352982B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-42ee668c66c54ecca5a8a6bf9f2152ae |
| Source note | uspto-grants-2002_03 |