HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658109Generated: November 3, 2026
Hydrazine hydrate (1:1) → HCID 12331717, compound
https://huagongshe.com/reaction/1658109
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21532623 | HCID 21532623 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12331717 | HCID 12331717 | — |
Reaction Steps
A solution of 11.0 g (0.02 mole) of 3,6-bis(4-diethylaminobutryl)-9-ethylcarbazole dihydrochloride and 25 ml of an 85% aqueous hydrazine hydrate solution is dissolved in 200 ml of ethylene glycol and heated to a temperature of 165°C for a period of 18 hours. The reaction mixture is cooled and diluted with water whereupon the free base of the desired compound separates as an oil. The product is separated by decantation, washed with water, dissolved in diethyl ether and the ethereal solution dried over magnesium sulfate. The dried solution is concentrated to a small volume and placed on an aluminum oxide chromatographic column and eluted with methylene chloride. The eluate is converted to its hydrochloride salt and crystallized from a methanol-ethyl acetate solution. Recrystallization from acetone with two additional recrystallizations from a methylene chloride-acetone solution results in the preparation of 3,6-bis(4-diethylaminobutyl)-9-ethylcarbazole dihydrochloride having a m.p. 172°-4° C; and λmaxEtOH 240; and E1cm1% 907.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03962451 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-33a11f9a7f09480cb43f181f280e02ba |
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| Source note | uspto-grants-1976_06 |
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