Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7H-Benzo[c]carbazole | HCID 67459 | — |
| Reactant | 2-Ethylhexyl bromide | HCID 86804 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66980816 | HCID 66980816 | — |
Reaction Steps
To 7H-benzo[c]carbazole (0.78 g, 3.59 mmol) in dimethylformamide (DMF) (4 ml) is added sodium hydride (0.21 g, 5.21 mmol) at 0° C., and the mixture is stirred for 1 hour. To the reaction mixture is added 1-bromo-2-ethylhexane (1.04 g, 5.39 mmol). The mixture is stirred at room temperature overnight, and then at 0° C. for 5 hours. After the reaction mixture is cooled at room temperature, it is poured into ice-water, and the crude product is extracted with AcOEt, and washed with water and brine. After drying over MgSO4 and concentration, the desired product is obtained as a brown liquid (1.21 g, 99%). The structure is confirmed by 1H-NMR spectrum (CDCl3) δ [ppm]: 0.83-0.92 (m), 1.20-1.43 (m), 2.07-2.10 (m), 4.24-4.38 (m), 7.37 (td), 7.44-7.50 (m), 7.52-7.54 (m), 7.62 (d), 7.69 (td), 7.87 (d), 7.99 (d), 8.59 (d), 8.80 (d)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051397B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-90d97ad4dd424c13b36995319df36383 |
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| Source note | uspto-grants-2015_06 |
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