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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533251Generated: October 26, 2026

2-Cyclohexen-1-one → ethyl 3-(3-oxocyclohexyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/533251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclohexen-1-oneHCID 13594—
ReactantEthyl indole-2-carboxylateHCID 73125—
ReactantBi(OTf)3HCID 9917655—
SolventAcetonitrileHCID 6342—
Productethyl 3-(3-oxocyclohexyl)-1H-indole-2-carboxylateHCID 67316060—

Reaction Conditions

Temperature65 °C

Reaction Steps

Ethyl 1H-indole-2-carboxylate (2.953 g) and cyclohex-2-enone (1.004 mL) were added to acetonitrile (50 mL). Bismuth (III) trifluoromethanesulfonate (341 mg) was added, and the solution was heated at 65° C. for two days. The solution was cooled, concentrated, and purified by flash column chromatography on silica gel with 10% increasing to 20% ethyl acetate in hexanes to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853209B2
Source datasetuspto-grants-2014_10
ORD IDord-a52a3c7e7b014a8cb21fba3f9ae58f16
Source noteuspto-grants-2014_10