Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloranil | HCID 8371 | — |
| Reactant | 5-Nitroindole | HCID 22523 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-methyl-5-nitro-1H-indole | HCID 15453462 | 80.4% |
Reaction Steps
To a solution of 5-nitroindole (from Aldrich, 0.82 g, 5.1 mmol) in 20 mL of dry THF was added 5.0 mL (15 mmol) of methylmagnesium bromide for 0.5 h period and the resulting reaction mixture was stirred for 1 h at 25° C. Reaction was the quenched by adding a THF solution of tetrachloro-1,4-benzoquinone (1.2 g, 4.9 mmol). Reaction mixture was concentrated in vacuo, yielding a dark solid which was subjected to column chromatography (30% EtOAc/n-Hexane) to yield 0.72 g (4.1 mmol, 80%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06303643B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-246718ab186c482a9733285c1dfae9aa |
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| Source note | uspto-grants-2001_10 |
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