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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55385Generated: October 28, 2026

Triethylamine → N-(2-ethoxy-5-hydroxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochloride

https://huagongshe.com/reaction/55385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Ethoxy-5-hydroxy-3,4,6-trimethylbenzyl chlorideHCID 19957711—
ReactantN-methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochlorideHCID 67726891—
SolventDimethylformamideHCID 6228—
ProductN-(2-ethoxy-5-hydroxy-3,4,6-trimethylbenzyl)-N-methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochlorideHCID 199576795%

Reaction Steps

N-Methyl-2-(4-hydroxy-2-isopropyl-5-methylphenoxy)ethylamine hydrochloride (10.4 g), 2-ethoxy-5-hydroxy-3,4,6-trimethylbenzyl chloride (9.15 g) and triethylamine (8.10 g) were dissolved in N,N-dimethylformamide (80 ml), and the mixture was stirred at room temperature for 4 hours. After the reaction, the solvent was distilled off and water was added. The mixture was extracted with ethyl acetate, and the extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The resulting liquid (1.0 g) was dissolved in methanol and conc. hydrochloric acid (0.2 ml) was added. The mixture was concentrated to dryness under reduced pressure. Recrystallization from ethanol-diethyl ether gave 910 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624961
Source datasetuspto-grants-1997_04
ORD IDord-90fae843b7e34b32be9273363dff04aa
Source noteuspto-grants-1997_04