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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55391Generated: October 30, 2026

2-(2-Isopropyl-5-methylphenoxy)ethanamine → N-(2-benzyloxy-5-ethoxy-3,4,6-trimethylbenzyl)-2-(2-isopropyl-5-methylphenoxy)ethylamine

https://huagongshe.com/reaction/55391

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Isopropyl-5-methylphenoxy)ethanamineHCID 425070—
Reactant2-Benzyloxy-5-ethoxy-3,4,6-trimethylbenzaldehydeHCID 19957707—
SolventBenzeneHCID 241—
ProductN-(2-benzyloxy-5-ethoxy-3,4,6-trimethylbenzyl)-2-(2-isopropyl-5-methylphenoxy)ethylamineHCID 1995771287.6%

Reaction Steps

A solution of 2-benzyloxy-5-ethoxy-3,4,6-trimethylbenzaldehyde (2.98 g) and 2-(2-isopropyl-5-methylphenoxy)ethylamine (1.93 g) in benzene (50 ml) was refluxed under heating for 5 hours in a Dean-Stark extractor. The solvent was distilled off under reduced pressure and the residue was suspended in ethanol (100 ml). Sodium borohydride (0.40 g) was added with ice-cooling and the mixture was stirred at room temperature for 16 hours. The solvent was distilled off under reduced pressure and water was added. The mixture was extracted with ethyl acetate and the obtained extract was purified by silica gel column chromatography (eluent; ethyl acetate/benzene=1/1) to give 4.16 g of a colorless solid. The solid was recrystallized from methanol to give 1.62 g of the title compound (colorless needle crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624961
Source datasetuspto-grants-1997_04
ORD IDord-17a85ff9583943e7b5d36306a9e9febb
Source noteuspto-grants-1997_04