Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-bromooctanoate | HCID 95580 | — |
| Reactant | HCID 21468934 | HCID 21468934 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21468829 | HCID 21468829 | 56.2% |
Reaction Steps
5-(2-Cyanophenyl)indole (5.04 mmoles, 1.1 g) in 70 ml THF was treated with sodium hydride (255 mg, 50% in mineral oil) and stirred at 0° C. for 30 minutes. Ethyl 2-bromooctanoate (5.5 mmoles) in 40 ml THF was added dropwise. The reaction was stirred at room temperature for 4 hours, cooled, poured onto ice, extracted with ethyl acetate. The organic phase was dried and concentrated. The intermediate was chromatographed over silica gel eluted with 20% ether in hexane. The reaction yielded 1.1 g of ethyl 2-[5-(2-cyanophenyl)indol-1-yl]octanoate. (MS)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05612360 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-4f189fe6aece4050a6c90bb8850489aa |
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| Source note | uspto-grants-1997_03 |
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