HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228309Generated: October 31, 2026
Potassium Carbonate → Tert-butyl 1-methyl-7-(4-methylphenyl)-2,3-dihydro-1-benzoazepine-4-carboxylate
https://huagongshe.com/reaction/2228309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18472450 | HCID 18472450 | — |
| Reactant | 4-Methylphenyl borate | HCID 86645333 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | Tert-butyl 1-methyl-7-(4-methylphenyl)-2,3-dihydro-1-benzoazepine-4-carboxylate | HCID 18472637 | 72% |
Reaction Steps
In water:ethanol:toluene (1:1:10, 18.0 ml) were dissolved 4-methylphenyl borate (276 mg) and tert-butyl 7-bromo-1-methyl-2,3-dihydro-1-benzoazepine-4-carboxylate (571 mg), and to the mixture was added potassium carbonate (560 mg). The mixture was stirred under argon atmosphere for 30 minutes, and to the mixture was added tetrakistriphenylphosphine palladium (78 mg). Under argon atmosphere, the mixture was refluxed for 19.5 hours. The mixture was diluted with ethyl acetate (300 ml) and washed with water (100 ml) and saturated brine (100 ml). The organic layer was dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified with silica gel column chromatography (120 g, hexane→hexane:ethyl acetate=10:1) to give tertbutyl 1-methyl-7-(4-methylphenyl)-2,3-dihydro-1-benzoazepine-4-carboxylate (422 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06413947B1 |
|---|
| Source dataset | uspto-grants-2002_07 |
|---|
| ORD ID | ord-1144c3efac41446da82adf32ccdcc476 |
|---|
| Source note | uspto-grants-2002_07 |
|---|