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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862402Generated: October 26, 2026

Water → (2,6-Dimethoxy-4-methylphenyl)(2-methylaminophenyl) Ketone

https://huagongshe.com/reaction/862402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-Methylisatoic anhydrideHCID 25160—
Reactant3,5-DimethoxytolueneHCID 77844—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product(2,6-Dimethoxy-4-methylphenyl)(2-methylaminophenyl) KetoneHCID 5732221678%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a solution of 30 g of 3,5-dimethoxytoluene in 400 ml of tetrahydrofuran are added, at a temperature in the region of -20° C., 129 ml of 1.6M butyllithium in hexane. Once the introduction is complete, the reaction mixture is brought to a temperature of 0° C. and is then stirred for 1 hour. It is cooled to -20° C. and 36.67 g of N-methylisatoic anhydride are added portionwise. The mixture is allowed to return to room temperature and is stirred over 2 hours, followed by addition of 500 ml of water and extraction with ethyl acetate. The organic phase is washed with water, dried over sodium sulphate and evaporated under vacuum. The residue is purified by chromatography on silica gel, eluent: toluene/ethyl acetate 9/1. The fractions of pure product are concentrated under vacuum and the residue is crystallized from isopropyl ether, filtered and dried. Beige crystals melting at 215° C. are obtained; Yield=78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719143
Source datasetuspto-grants-1998_02
ORD IDord-47e41d771d9c4d0280e185636e9a06cc
Source noteuspto-grants-1998_02