HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981818Generated: October 30, 2026
Acetic Acid → 2-(beta-Hydroxyethoxyethyl)amino-6-(beta-hydroxyethoxyethyl)aminonitrobenzene
https://huagongshe.com/reaction/981818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Chloro-2-(beta-hydroxyethoxyethyl)amino-6-(beta-hydroxyethoxyethyl)aminonitrobenzene | HCID 20071094 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(beta-Hydroxyethoxyethyl)amino-6-(beta-hydroxyethoxyethyl)aminonitrobenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04992586 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-e060d626c40d42b8a045574c9ed3b87c |
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| Source note | uspto-grants-1991_02 |
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