HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466603Generated: October 27, 2026
Acetic Acid → 4-Methylene-2-oxo-3-phenyl-1-oxa-3,8-diazaspiro[4,5]decane
https://huagongshe.com/reaction/466603
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 8-Formyl-4-methylene-2-oxo-3-phenyl-1-oxa-3,8-diazaspiro[4,5]decane | HCID 19814333 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methylene-2-oxo-3-phenyl-1-oxa-3,8-diazaspiro[4,5]decane | HCID 19814277 | 41% |
Reaction Steps
A solution containing 5.4 g of 8-formyl-4-methylene-2-oxo-3-phenyl-1-oxa-3,8-diazaspiro[4,5]decane, 3.0 g of hydrazine monohydrate and 3.6 g of acetic acid in 54 ml of aqueous ethanol of 60% by volume concentration is stirred under argon at a temperature of 62°-65° C. The reaction is followed by TLC. After termination of the reaction the mixture is evaporated under reduced pressure. After taking up the residue in chloroform and saturated aqueous sodium hydrogen carbonate solution, the chloroformic phase is separated, washed to neutral, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The crude product obtained is recrystallized from ethyl acetate under clarifying by activated carbon to give the title compound in 41.0% yield, m.p.: 185°-186° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157038 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-46c053b4f2f64a24ac72f036107fc2ef |
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| Source note | uspto-grants-1992_10 |
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