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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606860Generated: November 1, 2026

2-Methoxyethanol → 4-(beta-Methoxyethoxy)-2-(beta-hydroxyethyl)amino-6-(beta-hydroxyethyl)aminonitrobenzene

https://huagongshe.com/reaction/1606860

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(beta-Hydroxyethyl)amino-6-(beta-hydroxyethyl)amino-4-chloronitrobenzeneHCID 20071091—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(beta-Methoxyethoxy)-2-(beta-hydroxyethyl)amino-6-(beta-hydroxyethyl)aminonitrobenzeneHCID 19851174—

Reaction Steps

0.09 mole (25 g) of 4-chloro-2-(β-hydroxyethyl)amino-6-(β-hydroxyethyl)aminonitrobenzene, synthesized in stage 1 of example 2, was added to a solution of 11.9 g of pelletized potash in 60 ml of 2-methoxyethanol and 25 ml of N-methylpyrrolidone and heated for 4 hours over a boiling water bath. The reaction medium was diluted with 350 ml of ice water and the desired product obtained by high pressure liquid chromatography (HPLC). About 150 ml of the aqueous solution obtained by dilution of the reaction medium were injected onto a C18RD chromatographic column (Instrument: Waters Prep 500). The desired product was eluted by a 40% methanol--60% water solution. After evaporation of the fractions containing the desired product, a dry extract was obtained which was recrystallized from isopropanol. After recrystallization, it melted at 116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863482
Source datasetuspto-grants-1989_09
ORD IDord-924f1e9b6d5943628af752863d032451
Source noteuspto-grants-1989_09