HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4203Generated: October 25, 2026
Hydrazine hydrate (1:1) → N,N-bis(1-Methylethyl)-1,2-ethanediamine, dihydrochloride
https://huagongshe.com/reaction/4203
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | 2-{2-[Di(propan-2-yl)amino]ethyl}-1H-isoindole-1,3(2H)-dione | HCID 231072 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N,N-bis(1-Methylethyl)-1,2-ethanediamine, dihydrochloride | HCID 12203001 | — |
Reaction Steps
A solution of 40.54 g (0.148 mole) of 2-[2-[[N,N-bis(1-methylethyl)amino]ethyl]-2H-isoindole-1,3-dione and hydrazine hydrate (85%, 11.8 g, 0.2 mole) in 400 ml of 95% ethanol was heated at reflux for 5 hours. The reaction mixture was allowed to cool to room temperature while standing overnight. A white solid formed. The reaction mixture was concentrated almost to dryness on the rotary evaporator. The residue was dissolved in chloroform and extracted with 10% sodium hydroxide. After removing chloroform, a brown oil was obtained. A portion of the oil was dissolved in methanol and converted to the dihydrochloride salt. After recrystallization from methanol-diethyl ether, 1.50 g (20%) of white crystalline product, m.p. 178°-182° C. (decomposition) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04724235 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-d69cadb84c1f457aa9645d6fe5e18d9e |
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| Source note | uspto-grants-1988_02 |
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