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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420998Generated: November 1, 2026

Cyclohexene → HCID 66657709, compound

https://huagongshe.com/reaction/420998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantHCID 66657620HCID 66657620—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 66657709HCID 66657709—

Reaction Conditions

Temperature135 °C

Reaction Steps

A mixture of 3-(2-ethoxycarbonylvinyl)-1-(4-isopropoxyphenyl)-5-(5-trifluoromethylpyridin-2-yl)indole-2-carboxylic acid ethyl ester (150 mg, 0.26 mmol, see step (c) above), Pd—C (10%), cyclohexene (1.2 mL) in absolute EtOH was heated under microwave irradiation at 135° C. for 1 h. The mixture was filtered through Celite® and the solids were washed with EtOAc. The combined filtrates were concentrated to give the sub-title compound. Yield 150 mg (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097623B2
Source datasetuspto-grants-2012_01
ORD IDord-2d872bc0bca746c39f1eab39fc16c530
Source noteuspto-grants-2012_01