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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298481Generated: October 29, 2026

Water → 2-Methyl-7-(4-dimethylaminophenyl)-1-indanone

https://huagongshe.com/reaction/2298481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant4-(Dimethylamino)phenylboronic acidHCID 2734344—
Reactant7-Bromo-2-methyl-2,3-dihydro-1H-inden-1-oneHCID 15869783—
Catalystpalladium(II) acetateHCID 167845—
CatalystTris(o-tolylphenyl)phosphineHCID 22172997—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Methyl-7-(4-dimethylaminophenyl)-1-indanoneHCID 1586978476.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Using a method similar to Example 22, 8.0 g (0.032 mol) of (2), 5.85 g (0.038 mol) of 4-dimethylaminophenylboronic acid and 7.4 g (0.07 mol) of sodium carbonate were placed in 122 ml of dimethoxyethane and 37 ml of water in the reaction vessel, the mixture was degassed a number of times and saturated with argon. 142 mg (0.6 mmol) of palladium acetate and 385 mg (1.3 mmol) of tris(o-tolylphenyl)phosphine were added and the reaction mixture was stirred for 4 hours at 80° C. After addition of 150 ml of water, the mixture was extracted 4 times with 100 ml each time of diethyl ether, the ether phase was washed twice with 50 ml each time of water and dried over magnesium sulfate. Removal of the solvent and column filtration through neutral aluminum oxide (dichloromethane) gave 6.5 g of 2-methyl-7-(4-dimethylaminophenyl)-1-indanone as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492539B1
Source datasetuspto-grants-2002_12
ORD IDord-4e822485e7e04e669202c02b0f11970a
Source noteuspto-grants-2002_12