HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383550Generated: October 30, 2026
Hydrazine hydrate (1:1) → 4-Methyl-6-phenyl-4,5-dihydropyridazin-3(2H)-one
https://huagongshe.com/reaction/383550
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-Methyl-4-oxo-4-phenylbutanoic acid | HCID 74492 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methyl-6-phenyl-4,5-dihydropyridazin-3(2H)-one | HCID 13901390 | 95% |
Reaction Steps
7.7 g (40 mmole) of 2-methyl-4-oxo-4-phenylbutanoic acid was added to a 100 ml single-necked round bottom flask followed by 3.0 ml (60 mmole) of hydrazine monohydrate and then 20 ml of reagent grade ethanol (100%, 95% of ethanol should be fine also). The flask was fitted with a reflux condenser and the reaction mixture was heated to reflux in an oil bath at 110 C (temperature of oil bath) and stirred for 2 h. The flask was then removed from the oil bath and the reaction mixture cooled to ambient temperature. The stir bar was removed and the solvent was evaporated in vacuo in a water bath at 45° C. The residue was then treated with 50 ml of Milli-Q water and stirred for 10 minutes to give a suspension. The precipitate was collected by filtering, washed with 100 ml of 2N NaHCO3, then washed with 60 ml Milli-Q water three times, and dried over a medium frit sintered glass funnel in vacuo to give 7.15 g of white crystals (Syn. ID, WH-8-004). Yield, 95%, confirmed by ESI-MS. ESI-MS: m/z 189.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367672B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-f0d891d3f94c4660913e5d07f395a947 |
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| Source note | uspto-grants-2013_02 |
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