HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838973Generated: October 31, 2026
Hydrazine hydrate (1:1) → 5-amino-1(2H)-phthalazinone
https://huagongshe.com/reaction/838973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 3-hydroxy-4-nitro-3H-isobenzofuran-1-one | HCID 11095528 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methane | HCID 297 | — |
| Product | 5-amino-1(2H)-phthalazinone | HCID 12341002 | 35% |
Reaction Steps
A stirred solution of 3-hydroxy-4-nitrophthalide (43.4 g, 0.22 mole) and hydrazine hydrate (11.6 ml) in ethanol (1830 ml) was heated under reflux for 1 hour. The heating was discontinued and palladium on carbon (10%, 2.44 g) was added (with caution) over 15 minutes. A solution of hydrazine hydrate (24.2 ml) in ethanol (304 ml) was then added, dropwise, over 30 minutes and the mixture was heated under reflux for a further 2.5 hours. Filtration of the hot reaction mixture followed by the addition of a saturated solution of hydrogen chloride in ethanol (80 ml) to the filtrate gave a solid precipitate which was collected and washed with ethanol and ether. Evaporation of the filtrate gave a solid residue which was washed several times with boiling ethanol. The combined solids were recrystallised from water, after charcoal treatment, to give 5-amino-1(2H)-phthalazinone (12.7 g, 35%, m.p. 289°-291°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093725 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-d33471de1fad43308040f87c3169361c |
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| Source note | uspto-grants-1978_06 |
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