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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483132Generated: October 25, 2026

Acetyl chloride → Indole

https://huagongshe.com/reaction/483132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant(2-Ethylphenyl)hydrazineHCID 2733210—
Reactant2-Carbomethoxymethyl-5-ethenyl-2-ethylcyclohexanoneHCID 14201434—
SolventMethanolHCID 887—
ProductIndoleHCID 79838%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578398
Source datasetuspto-grants-1986_03
ORD IDord-b6e21d77676643a9a84bb7d23940e5fa
Source noteuspto-grants-1986_03