HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5,6-dihydro-5-oxo-11H-indeno [1,2-c]isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Homophthalic anhydride | HCID 12801 | — |
| Reactant | 2-(Bromomethyl)benzonitrile | HCID 89599 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5,6-dihydro-5-oxo-11H-indeno [1,2-c]isoquinoline | HCID 10105388 | — |
Reaction Steps
To a solution of homophthalic anhydride (324 mg, 2.0 mmol) in acetonitrile (15 mL) was added 2-cyanobenzyl bromide (431 mg, 2.0 mmol, 1.0 eq) and triethylamine (5 mL). The reaction was stirred under inert atmosphere at room temperature for 30 minutes, after which time a yellow precipitate appeared. The reaction mixture was then heated at reflux for 18 h and the resulting white precipitate was filtered, washed using acetonitrile (3×8 mL) and dried under vacuum to provide Compound 13a as a white crystalline solid. Yield=150 mg (32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956035B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-8c9830ebd5bf43b5b84b086fcbd83943 |
| Source note | uspto-grants-2005_10 |