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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862937Generated: October 30, 2026

Ethyl(RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindene-2-carboxylate → Ethyl (RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylate

https://huagongshe.com/reaction/862937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl(RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindene-2-carboxylateHCID 18969642—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl (RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylateHCID 5383497765%

Reaction Steps

To a solution of ethyl(RS)-1-(3,4-methylenedioxyphenyl)-3-phenylindene-2-carboxylate (1.00 g, 2.60 mmol) in EtOH (25 ml) was added 10% palladium on activated carbon (30 mg). The resulting suspension was stirred under an atmosphere of H2 overnight. Thin layer chromatographic analysis indicated that the reaction was incomplete, so additional 10% palladium on activated carbon (30 mg) was added, and the mixture was shaken on a Parr hydrogenator at 30 psi H2 for 2 d. At this time, thin layer chromatographic analysis again indicated that the reaction was incomplete. The reaction mixture was filtered through a pad of Celite, and 10% palladium on activated carbon (250 mg) was added. The reaction mixture was shaken on a Parr hydrogenator at 60 psi H2 overnight. Filtration and repetition of the latter hydrogenation conditions led to complete consumption of starting material. The reaction mixture was filtered through a pad of Celite, and the filtrate was concentrated under reduced pressure to afford the title compound (650 mg, 65%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719182
Source datasetuspto-grants-1998_02
ORD IDord-e3c99ac94db8409dae7e87286c4d78fc
Source noteuspto-grants-1998_02