Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837684Generated: November 2, 2026

Water → HCID 22678633, compound

https://huagongshe.com/reaction/1837684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantHCID 22678559HCID 22678559—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 22678633HCID 22678633—

Reaction Steps

20.3 g of 4-(1-benzyl)piperidinecarboxaldehyde and 48.0 g of (2,3-methylenedioxybenzyl)triphenylphosphonium bromide and 12.0 g of potassium tert-butoxide were suspended in 200 ml of N,N-dimethylformamide, and the mixture was stirred at room temperature for one hour. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the crude product was purified and separated by NH form silica gel column chromatography (ethyl acetate:hexane=1:4). The resulting product and 2.03 g of 10% palladium-carbon powder (water-containing product) were suspended in 200 ml of ethanol. After replacing the atmosphere of a container with hydrogen, the mixture was stirred at room temperature under ordinary atmosphere for two hours. The reaction solution was filtered, and the filtrate was evaporated, to give 20.3 g of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784192B2
Source datasetuspto-grants-2004_08
ORD IDord-3114c3d0058b4d109a77c97ca0f7bbba
Source noteuspto-grants-2004_08