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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494935Generated: October 30, 2026

Toluene → 2,3-Dihydro-5-methoxy-2,2-dimethyl-1H-inden-1-one

https://huagongshe.com/reaction/494935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Methoxyindan-1-oneHCID 78787—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
SolventEthyl AcetateHCID 8857—
Product2,3-Dihydro-5-methoxy-2,2-dimethyl-1H-inden-1-oneHCID 10330158—

Reaction Steps

7.78 g of potassium t-butoxide was dissolved in 66.3 ml of t-butanol and 150 ml of toluene. Thereafter, 5.00 g of 5-methoxyindanone dissolved in 170 ml of toluene was added dropwise to the reaction solution at room temperature. Approximately 10 minutes later, 4.79 ml of methyl iodide was added to the reaction solution. After completion of the reaction, a saturated ammonium chloride aqueous solution and ethyl acetate were added to the reaction solution, so as to separate an organic layer. The organic layer was then dried over anhydrous magnesium sulfate. After the organic layer had been filtered through celite, the drying agent was removed by filtration. Thereafter, the organic layer was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain 2.08 g of 5-methoxy-2,2-dimethylindanone. The obtained product was dissolved in 9 ml of methanesulfonic acid. Then, 2.45 g of methionine was added to the reaction solution, and the obtained mixture was heated to 110° C. After completion of the reaction, a saturated sodium chloride aqueous solution and ethyl acetate were added to the reaction solution, so as to separate an organic layer. The organic layer was then dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain 1.41 g of the subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538123B2
Source datasetuspto-grants-2009_05
ORD IDord-f1168b0a92c743e59179787c4a3444bc
Source noteuspto-grants-2009_05