HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-Bromoethyl)benzene → ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-Bromoethyl)benzene | HCID 11454 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | ethyl 2-methyl-1H-indole-3-carboxylate | HCID 4072358 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate | HCID 89740220 | 56.1% |
Reaction Steps
A mixture of ethyl 2-methyl-1H-indole-3-carboxylate (400 mg, 1.97 mmol) and sodium hydride (47 mg, 2.0 mmol) in N,N-dimethylformamide (5.0 mL) was stirred at room temperature for 0.5 hours, and then (1-bromoethyl)benzene (361 mg, 2.0 mmol) was added. The mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into ice-cold water and extracted with ethyl acetate. Organic layers were combined and concentrated to give a residue. The residue was purified by chromatography (petroleum ether/ethyl acetate 5:1) to give ethyl 2-methyl-1-(1-phenylethyl)-1H-indole-3-carboxylate (340 mg, 56%). LRMS (M+H+) m/z: calcd 307.16. found 307.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09371331B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-824e13e84ae64d5f94a0eee41f3512dc |
| Source note | uspto-grants-2016_06 |