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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291443Generated: November 1, 2026

Acetic Acid → 2-(beta-Hydroxyethoxyethyl)amino-6-(beta-hydroxyethoxyethyl)aminonitrobenzene

https://huagongshe.com/reaction/2291443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
Reactant4-Chloro-2-(beta-hydroxyethoxyethyl)amino-6-(beta-hydroxyethoxyethyl)aminonitrobenzeneHCID 20071094—
CatalystPalladiumHCID 23938—
SolventTriethylamineHCID 8471—
Product2-(beta-Hydroxyethoxyethyl)amino-6-(beta-hydroxyethoxyethyl)aminonitrobenzeneHCID 54067877—

Reaction Steps

300 mg of palladium at a concentration of 10% on calcium carbonate are added to 0.015 mole (5.45 g) of 4-chloro-2-(β-hydroxyethoxyethyl)amino-6-(β-hydroxyethoxyethyl)aminonitrobenzene in 11 ml of triethylamine. 1.1 ml of acetic acid and 2.05 ml of formic acid are then run in dropwise. When the additions have been completed the reaction mixture is heated under reflux for 30 minutes. 10 ml of water are added. The reaction mixture diluted in this manner is filtered hot to remove the catalyst. The filtrate is evaporated to dryness under vacuum in the presence of absolute ethanol and the residue is taken up with ethyl acetate. Insoluble organic salts are removed by filtration. The ethyl acetate is evaporated off to dryness. Acetonitrile and then water are added to the residue. The expected product precipitates. Recrystallized from ethyl acetate, it melts at 82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797129
Source datasetuspto-grants-1989_01
ORD IDord-2cb439cb550d4989935b3818d9d62153
Source noteuspto-grants-1989_01