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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500332Generated: October 30, 2026

Ammonium formate → HCID 86633674, compound

https://huagongshe.com/reaction/1500332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantChloroform methanolHCID 21584188—
ReactantHCID 68408396HCID 68408396—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 86633674HCID 8663367474%

Reaction Steps

1.5 g 20% Pd(OH)2/C and 6.95 g (3 eq) ammonium formate were added to a solution of 10 g (1 eq) 1-benzyl-4-butyl-N,N-dimethylpiperidin-4-amine in 100 ml MeOH. The reaction mixture obtained was refluxed for 30 min. The reaction course was monitored by thin-layer chromatography (20% MeOH/CHCl3). Once the conversion was complete, the reaction solution was cooled to room temperature, filtered over celite and rewashed with methanol. The methanol is distilled off, the residue taken up in ethyl acetate/hexane, the solvent decanted off and toluene added. The organic phase thus obtained was concentrated under reduced pressure and the residue taken up in 150 ml dichloromethane. HCl gas was passed through the dichloromethane solution for 20 min, the solvent was distilled off and 7 g (74%) of product were obtained in this way as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206156B2
Source datasetuspto-grants-2015_12
ORD IDord-5f7aa74baff646d58e6b7bdba1e368cc
Source noteuspto-grants-2015_12