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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400692Generated: October 29, 2026

1,5,6,7-Tetrahydro-4H-indol-4-one → HCID 60026304, compound

https://huagongshe.com/reaction/400692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5,6,7-Tetrahydro-4H-indol-4-oneHCID 280229—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 57809800HCID 57809800—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 60026304HCID 6002630458%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a suspension of 7-[1,1-dimethyl-2-(2-trifluoromethyloxiranyl)ethyl]-5-methanesulfonyl-2,3-dihydrobenzofuran (101 mg, 0.33 mmol) and 1,5,6,7-tetrahydroindol-4-one (74.9 mg, 0.56 mmol) in 0.75 mL of anhydrous ethanol was added sodium ethoxide (21 wt. % solution in ethanol, 103 μL). After heating at 85° C. for 16 hours, the reaction mixture was diluted with ethyl acetate, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by column chromatography with silica gel (eluted with 50% to 60% ethyl acetate-hexanes) to give 80.0 mg (58% yield) of the title compound as a white solid, m.p. 207° C.-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-12c7a7db30cc441eaf0a68e5e825fbf3
Source noteuspto-grants-2014_06