Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Acetylpyridine | HCID 9589 | — |
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 44554133 | HCID 44554133 | — |
Reaction Steps
To a solution of 4-bromophenylhydrazine hydrochloride (11.5 g, 50 mmol) in anhydrous ethanol (200 mL) is added 3-acetylpyridine (6.1 g, 50 mmol). The mixture is heated to 90° C. and stirred for 3 h, cooled to room temperature and filtered through a sintered glass funnel. The solid is washed with ethanol and placed under high vacuum overnight to give N-(4-bromo-phenyl)-N′-[1-pyridin-3-yl-eth-(Z)-ylidene]-hydrazine hydrochloride as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030334B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-2f1b2049363849f7a23ca9085ff8bb19 |
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| Source note | uspto-grants-2011_10 |
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