HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298808Generated: October 30, 2026
HCID 18378604, compound → HCID 18378582, compound
https://huagongshe.com/reaction/2298808
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18378604 | HCID 18378604 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18378582 | HCID 18378582 | 21.8% |
Reaction Steps
To a solution of methyltriphenylphosphonium bromide (607 mg) in N,N-dimethylformamide (10 ml) was added potassium-tert-butoxide (191 mg), and the mixture was stirred at room temperature for 30 minutes. Methyl 2-methoxy-4-(2,3,4,5-tetrahydro-5-oxo-1H-1-benzazepin-1-yl)carbonylbenzoate (300 mg) was added to the resulting solution, and the mixture was stirred at room temperature overnight. The mixture was diluted with ethyl acetate and the solution was washed successively with 1N hydrochloric acid, water and brine. The organic layer was dried over magnesium sulfate and the solvent was evaporated in vacuo to give an oil. The crude product was purified by silica gel column chromatography (10% ethyl acetate in hexane) to give methyl 2-methoxy-4-(2,3,4,5-tetrahydro-5-methylene-1H-1-benzazepin-1-yl)carbonylbenzoate (65 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06495542B1 |
|---|
| Source dataset | uspto-grants-2002_12 |
|---|
| ORD ID | ord-5b8a3695cbad4e34b66b2498c4c82f7e |
|---|
| Source note | uspto-grants-2002_12 |
|---|