HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 8-Methoxy-6H-11-oxa-6-aza-benzo[a]fluoren-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Hydroxy-5-methoxybenzonitrile | HCID 7022529 | — |
| Reactant | alpha-Bromodimethylhomophthalate | HCID 131725194 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 8-Methoxy-6H-11-oxa-6-aza-benzo[a]fluoren-5-one | HCID 11637529 | — |
Reaction Steps
α-Bromodimethylhomophthalate (20a) (1.16 g) and 2-hydroxy-5-methoxy-benzonitrile (0.6 g, 4 mmol, 1 eq) were dissolved by warming in acetonitrile (6 mL). Triethylamine (5.6 mL, 10 eq) was then added and the reaction was heated at reflux for 48 h under inert atmosphere, then cooled to room temperature. The reaction mixture was diluted with saturated sodium bicarbonate (40 mL) and the resulting suspension was allowed to stir for 2 h, and was then filtered. The filtercake was washed sequentially with 1 N HCl (2×50 mL), acetonitrile (2×50 mL) and dichloromethane (50 mL), then dried in a vacuum oven at 50° C. for three days to provide Compound 22a as an white solid. Yield=0.81 g (76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956035B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-0784b5b5b0464a1b9470530301fef300 |
| Source note | uspto-grants-2005_10 |