Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 5-Bromoindole-2-carboxylate | HCID 259091 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21964305 | HCID 21964305 | — |
Reaction Steps
NaH (60%, 3.88 g, 96.98 mmol) was added portionwise to a stirring solution of ethyl 5-bromo-1H-indole-2-Carboxylate (20.0 g, 74.6 mmol) in DMF (140 mL) at 0° C. under a nitrogen atmosphere over a period of 10 min. The mixture was then warmed to room temperature. After the reaction mixture was stirred at room temperature for one hour, 4-methylbenzyl bromide (14.2 g, 74.6 mmol) was added and the mixture was stirred at room temperature overnight. The reaction was quenched with aqueous ammonium chloride and diluted with water. The aqueous mixture was extracted with ethyl acetate. The organic extract was washed with water and brine, dried over anhydrous magnesium sulfate. This mixture was concentrated to give a semi-solid contained 0.8 mole equivalent DMF. Mass spectrum (ESI, [M+H]+) m/z 372. 1H NMR (400 MHz, DMSO-d6) δ 7.93 (d, 1H, J=7.94 Hz), 7.55 (d, 1H, J=9.01 Hz), 7.40 (dd, 1H, J=8.85 and 1.98 Hz), 7.32 (s, 1H), 7.04 (d, 2H, J=7.96 Hz), 6.90 (d, 2H, J=7.94 Hz), 5.79 (s, 2H), 4.28 (q, 2H), 2.20 (s, 3H), and 1.28 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101903B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-d255c02a742e4920b85803b7e010b081 |
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| Source note | uspto-grants-2006_09 |
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