Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,3-Dimethyl-6-nitro-1,3-dihydro-2H-indol-2-one | HCID 13589227 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69071675 | HCID 69071675 | 87.1% |
Reaction Steps
A solution of 3,3-dimethyl-6-nitro-1,3-dihydro-indol-2-one (6 g, 29.10 mmol) in anhydrous N,N-dimethylformamide (DMF) (35 ml) was treated with sodium hydride. The resulting suspension was stirred for 1 h at 60° C. A solution of bromo-ethane (2.17 mL, 3.17 g, 29.10 mmol) in DMF (10 ml) was added. The mixture was allowed to cool to room temperature and stirred for 1 h. After removal of the solvent the mixture was quenched with water (100 ml) and extracted with ethyl acetate (3×100 ml). The extract was dried over Na2SO4, evaporated and the crude product was purified by column chromatography on silica gel. Elution with ethyl acetate/n-heptane (1:3) yielded 5.94 g (87%) of a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07462639B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-e8530b8b78884fb8aba16e8c3cb04d5b |
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| Source note | uspto-grants-2008_12 |
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