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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269475Generated: October 31, 2026

Semicarbazide hydrochloride → HCID 72440645, compound

https://huagongshe.com/reaction/1269475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSemicarbazide hydrochlorideHCID 11236—
Reactant2,6-Diethyl-2,3,6-trimethyl-1-(1-phenylethoxy)piperidin-4-oneHCID 22341848—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
ProductHCID 72440645HCID 7244064598.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199245B2
Source datasetuspto-grants-2007_04
ORD IDord-774c324ca0e14caa8d4eef541da34bac
Source noteuspto-grants-2007_04