Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 5-Nitro-2-phenyl-1H-indole | HCID 280309 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67285626 | HCID 67285626 | — |
Reaction Steps
To a solution of 2-phenyl-5-nitroindole (prepared as described in J. Org. Chem. (1966), 31(1), 65-9) (1.5 g; 6.3 mmol) in CH3CN (50 ml) was added K2CO3(1.7 g; 12.6 mmol). To the mixture thus obtained was then added dropwise ethyl 4-bromobutanoate (3.3 g; 16 mmol) and the resulting mixture was heated to 120° C. under stirring for 18 hours. After cooling, the mixture was poured into water (500 ml) and the crude product was filtered, dried under vacuum to give ethyl 4-(5-nitro-2-phenyl-1H-indol-1-yl)butanoate which was used in the following reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399477B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-c135769ca83f41e48415971ebd3ba03f |
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| Source note | uspto-grants-2013_03 |
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