Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2a,3,4,5-Tetrahydrobenzo[cd]indol-2(1H)-one | HCID 599375 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22449318 | HCID 22449318 | 70% |
Reaction Steps
(RS)-2a,3,4,5-tetrahydro-1H-benz[cd]indol-2-one(3.46 g, 20 mmol) was dissolved in anhydrous N,N,-dimethylformamide (20 ml). Then, 60% sodium hydride (0.8 g, 20 mmol) was added thereto and the resulting mixture was stirred at room temperature for 1 hour. Successively the reaction mixture obtained was cooled to −20° C., and ethyl 3-bromo propionate (2.55 ml, 20 mmol) was added thereto. The resulting mixture was stirred at room temperature for further 1 hour. Ethyl acetate and water were added thereto to extract a reaction product. The ethyl acetate solution was washed with saturated saline solution and then dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure to obtain a reaction product. Thereafter, diisopropyl ether was added to the resulting reaction product to crystallized the same. Thus, the above-described object compound was obtained in an amount of 3.80 g (yield 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06407112B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-56a4298cafd4430ba0cdbfad81ec8c76 |
|---|
| Source note | uspto-grants-2002_06 |
|---|