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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279311Generated: November 2, 2026

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

https://huagongshe.com/reaction/1279311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl(RS)-1-(3,4-Methylenedioxyphenyl)-3-phenylindene-2-carboxylateHCID 18969642—
Reactant1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylateHCID 21714789—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylic acidHCID 2171479065%

Reaction Steps

Ethyl (1RS, 2SR, 3SR)-1-(3,4-Methylenedioxyphenyl)-3-phenylindane-2-carboxylate. 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 numberUS06448260B2
Source datasetuspto-grants-2002_09
ORD IDord-420ff242cdb643b7936aabb208e5123f
Source noteuspto-grants-2002_09