HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042006Generated: October 30, 2026
Ammonium Hydroxide → 1-Chloro-4-hydrazinophthalazine
https://huagongshe.com/reaction/1042006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1,4-Dichlorophthalazine | HCID 78490 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Chloro-4-hydrazinophthalazine | HCID 2793752 | 84% |
Reaction Steps
A mixture of 1,4-dichlorophthalazine 23 (10.2 g, 51.2 mmol) and ammonium hydroxide (4.5 mL) in ethanol (110 mL) was heated to 60° C. Hydrazine hydrate (9 mL, 179 mmol) was added dropwise. After about one-half of the hydrazine hydrate was added, a thick precipitate formed. The mixture was stirred well and the temperature was kept below 74° C. by controlled addition of reagent. After the addition was complete the reaction was heated at reflux for 10 min, then allowed to cool. The reaction was filtered and the solids were washed with water (20 mL) and ethanol (20 mL), then dried at 40° C. in a vacuum oven overnight. The crude material was recrystallized from acetonitrile to afford 8.38 g (84%) of 11 as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557815B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-84d9e838625342caa8890767ce8c4dde |
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| Source note | uspto-grants-2013_10 |
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