HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217864Generated: October 30, 2026
Ethanol → 2,4-Dihydro-4-(4-piperidinyl)-3H-1,2,4-triazol-3-one
https://huagongshe.com/reaction/2217864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1,4-Cyclohexadiene | HCID 12343 | — |
| Reactant | 4-(1-Benzyl-4-piperidinyl)-3,4-dihydro-2H-1,2,4-triazole-3-one | HCID 59175734 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Dihydro-4-(4-piperidinyl)-3H-1,2,4-triazol-3-one | HCID 68502202 | 50.3% |
Reaction Steps
2,4-Dihydro-4-[1-(phenylmethyl)-4-piperidinyl]-3H-1,2,4-triazol-3-one (Example 64(b)) (2.2 g) was divided between 2, 10 mL vials. 1,4-Cyclohexadiene (5 mL) and palladium hydroxide (270 mg, 20 wt. % on carbon) were added to each vial and the reactions were heated at 100° C. for 30 minutes within a microwave. The reaction mixtures were combined, ethanol (50 mL) and water (50 mL) were added and the mixture was filtered through diatomaceous earth and evaporated to give the sub-title compound as a solid (720 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07408065B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-64fb7b54e25f48c6b0e8d4b12a465203 |
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| Source note | uspto-grants-2008_08 |
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