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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55387Generated: October 27, 2026

Triethylamine → N-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine

https://huagongshe.com/reaction/55387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(Chloromethyl)-2,5-dimethoxy-3,4,6-trimethylbenzeneHCID 10878929—
ReactantN-Methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamineHCID 19957678—
SolventDimethylformamideHCID 6228—
ProductN-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamineHCID 1995765875%

Reaction Steps

N-Methyl-2-(4-acetylamino-2-isopropyl-5-methylphenoxy)ethylamine (4.94 g) and 2,5-dimethoxy-3,4,6-trimethylbenzyl chloride (4.29 g) were dissolved in N,N-dimethylformamide (70 ml), and triethylamine (1.89 g) was added dropwise while stirring the mixture at room temperature. The mixture was stirred at room temperature for 16.5 hours. After the reaction, the solvent was distilled off, and water was added. The mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained crude product was purified by silica gel chromatography (eluent; ethyl acetate/benzene=1/1) to give 6.40 g of a pale-yellow solid. A portion (1.0 g) was taken therefrom and recrystallized from diisopropyl ether to give 0.62 g of the title compound (colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624961
Source datasetuspto-grants-1997_04
ORD IDord-f9a8a70d8a224fc19a8a03acae303de4
Source noteuspto-grants-1997_04