Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | (2-Ethylphenyl)hydrazine | HCID 2733210 | — |
| Reactant | 2-Carbomethoxymethyl-5-ethenyl-2-ethylcyclohexanone | HCID 14201434 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Indole | HCID 798 | 38% |
Reaction Steps
The more polar ketone isomer of 2-carbomethoxymethyl-5-ethenyl-2-ethylcyclohexanone (5.084 g, 22.66 mmol) and the 2-ethylphenylhydrazine (3.086 g, 22.66 mmol) were heated at reflux in 97 ml of methanol under nitrogen for 48 hours. The reaction was then cooled to 0° C., treated with 45.32 mmol (3.56 g, 3.22 ml) of AcCl and refluxed an additional 45 minutes. Cooling, concentration and flash chromatography afforded 2.772 g (8.52 mmol, 38%) of indole as an orange oil. Rf =0.47 in 15% ethyl acetate/petroleum ether on TLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04578398 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-b6e21d77676643a9a84bb7d23940e5fa |
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| Source note | uspto-grants-1986_03 |
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