HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981823Generated: October 30, 2026
Acetic Acid → 2-(beta-Diethylaminoethyl)amino-6-(beta-diethylaminoethyl)aminonitrobenzene dihydrochloride
https://huagongshe.com/reaction/981823
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chloro-2-(beta-diethylaminoethyl)amino-6-(beta-diethylaminoethyl)aminonitrobenzene | HCID 20071086 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(beta-Diethylaminoethyl)amino-6-(beta-diethylaminoethyl)aminonitrobenzene dihydrochloride | HCID 20071084 | — |
Reaction Steps
300 mg of palladium at a concentration of 10% on calcium carbonate are added to 0.015 mole (5.8 g) of 4-chloro-2-(β-diethylaminoethyl)amino-6-(β-diethylaminoethyl)aminonitrobenzene in 11.1 ml of triethylamine, after which 2.86 ml of acetic acid and 2.1 ml of formic acid are added dropwise. After the end of the additions, the materials are heated under reflux for 3 hours 30 minutes. The reaction mixture is diluted with 10 ml of water. The catalyst is removed by hot filtration. The filtrate is evaporated to dryness under vacuum. The inorganic salts are precipitated by adding acetone and are removed by filtration. After evaporation of the acetone, an oil is obtained and this, after treatment with a solution of hydrochloric acid in absolute ethanol, leads to the expected product which is isolated by evaporating off the alcohol and precipitating with ethyl ether.
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-42e6791221cd44598a61d509f76afd30 |
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| Source note | uspto-grants-1991_02 |
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