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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220165Generated: October 29, 2026

5-Methoxy-6-methyl-1H-indene-3-carbonitrile → 6-Methoxy-5-methyl-2,3-dihydro-1H-indene-1-carbonitrile

https://huagongshe.com/reaction/2220165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methoxy-6-methyl-1H-indene-3-carbonitrileHCID 45091355—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
Product6-Methoxy-5-methyl-2,3-dihydro-1H-indene-1-carbonitrileHCID 4509140591.6%

Reaction Steps

Under a nitrogen atmosphere, 0.1 gram (catalyst) of 10% palladium on carbon and 0.05 gram (catalyst) of 5% platinum on carbon were placed in a 250 mL Parr hydrogenation bottle, followed by a solution of 2.5 grams (0.014 mole) of 5-methoxy-6-methylinden-3-carbonitrile (iii) in 100 mL of ethyl acetate. The mixture was hydrogenated in a Parr hydrogenation apparatus for about 45 minutes, during which time the theoretical amount of hydrogen was taken up by the reaction. The reaction mixture was then washed through a pad of diatomaceous earth with methylene chloride. The methylene chloride wash was concentrated under reduced pressure, yielding 2.4 grams of subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417057B2
Source datasetuspto-grants-2008_08
ORD IDord-61f3ffebb77f4409b67f9643101f0447
Source noteuspto-grants-2008_08