HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269475Generated: October 31, 2026
Semicarbazide hydrochloride → HCID 72440645, compound
https://huagongshe.com/reaction/1269475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Semicarbazide hydrochloride | HCID 11236 | — |
| Reactant | 2,6-Diethyl-2,3,6-trimethyl-1-(1-phenylethoxy)piperidin-4-one | HCID 22341848 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 72440645 | HCID 72440645 | 98.8% |
Reaction Steps
2,6-diethyl-2,3,6-trimethyl-1-(1-phenyl-ethoxy)-4-oxopiperidine prepared according to DE 199 09 767 A1 is dissolved in methanol containing 10% by weight of KOH and stirred for 5 hours at room temperature. Methanol is evaporated, the residue is washed with water and dried in vacuo. To a solution of 6.4 g (0.02 mol) 2,6-diethyl-2,3,6-trimethyl-1-(1-pheyl-ethoxy)-piperidine-4-one in 20 ml methanol are added 3.3 g (0.03 mol) semicarbazide hydrochloride and 1.67 g (0.025 mol) KOH (85%). The mixture is stirred under reflux 5 h and then diluted with 200 ml water. The precipitate is extracted into 100 ml of dichloromethane, the organic layer is washed with water, dryied over MgSO4 and evaporated to give 7.8 g (98.8%) of the title compound as a slightly yellow resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07199245B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-774c324ca0e14caa8d4eef541da34bac |
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| Source note | uspto-grants-2007_04 |
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