HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 22247351, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Iodooctane | HCID 12380 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 69628847 | HCID 69628847 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22247351 | HCID 22247351 | — |
Reaction Steps
5-Bromo-7-methyl-7-nitroindoline (3.6 g) was dissolved in N,N-dimethylformamide (36 ml), and sodium hydride (677 mg) was added, which was followed by stirring at room temperature for 0.5 hr. 1-Iodooctane (3.4 g) was added to the reaction mixture and the mixture was stirred at the same temperature for 24 hr. Ethyl acetate (200 ml) was added to the reaction mixture, and the mixture was washed with water and dried over anhydrous sodium sulfate. Ethyl acetate was evaporated under reduced pressure. The residue was purified by gel column chromatography (eluent: ethyl acetate/n-hexane=1/100−1/50) to give 4.0 g of oily 1 -octyl-5-bromo-6-methyl-7-nitroindoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06200988B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-360539f620a94ea08b57346e5faa13e2 |
| Source note | uspto-grants-2001_03 |