HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270169Generated: October 30, 2026
Hydrazine hydrate (1:1) → HCID 9877790, compound
https://huagongshe.com/reaction/270169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21964329 | HCID 21964329 | — |
| Reactant | HCID 21964340 | HCID 21964340 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 9877790 | HCID 9877790 | — |
Reaction Steps
To a mixture of 2-(5-methyl-8-oxo-8H-2-thia-cyclopenta[a]inden-1-yl)-isoindole-1,3-dione and 2-(7-methyl-8-oxo-8H-2-thia-cyclopenta[a]inden-1-yl)-isoindole-1,3-dione (0.45 mmol, Example & 3, Part E) in absolute ethanol (5 mL) was added hydrazine hydrate (0.5 mmol). The suspension was heated to reflux for one hour, cooled to room temperature, concentrated in vacuo, and the residue dissolved in methylene chloride. The solution was chilled to 5° C. for one hour, during which time the phthaloyl hydrazide precipitated. The precipitate was removed by filtration, the filtrate concentrated in vacuo, and the residue purified by column chromatography on silica gel, eluting with a 4:1 mixture of petroleum ether:ethyl acetate. Fractions containing the individual products were pooled, evaporated, and each product was isolated after recrystallization from petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449490B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-40e8d02c85614839ade2b64a1f6ec703 |
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| Source note | uspto-grants-2008_11 |
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