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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980840Generated: November 1, 2026

Water → N-(1,1-dimethyl-4-indanyl)-o-methylbenzamide

https://huagongshe.com/reaction/1980840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-Methylbenzoyl chlorideHCID 70276—
Reactant1,1-Dimethyl-2,3-dihydro-1H-inden-4-amineHCID 13115615—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-(1,1-dimethyl-4-indanyl)-o-methylbenzamideHCID 1326804393.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.81 g of o-methylbenzoyl chloride (5.25 m mol) in 3 ml of tetrahydrofuran is added dropwise to a solution of 0.81 g of 1,1-dimethyl-4-aminoindan (5.00 m mol) and 0.61 g of triethylamine (6.00 m mol) in 10 ml of tetrahydrofuran, while maintaining the reaction mixture at 0° C. by ice-cooling. Then, reaction mixture is stirred over night at room temperature, and water and ethyl acetate are added to the mixture. The organic layer is washed with 5% hydrochloric acid and water and dried over anhydrous sodium sulfate. After the solvent is removed by distillation, the residue is dried to give 1.31 g of N-(1,1-dimethyl-4-indanyl)-o-methylbenzamide (yield: 93.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04511581
Source datasetuspto-grants-1985_04
ORD IDord-f3a9a146354041b1b3b03d921da5ed0a
Source noteuspto-grants-1985_04