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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220838Generated: October 31, 2026

Acetic Acid → Benzyl 4-((cyclopropylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/220838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopropylamineHCID 69828—
ReactantBenzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductBenzyl 4-((cyclopropylamino)methyl)piperidine-1-carboxylateHCID 5755543247%

Reaction Steps

Cyclopropylamine (1.4 g, 24.4 mmol) and acetic acid (0.5 ml) were added to a solution of 4-formyl-piperidine-1-carboxylic acid benzyl ester from Example E33.2 (5.5 g, 22.2 mmol) in methanol (49.5 ml) and the mixture was stirred for 1 h at room temperature. Sodium cyanoborohydride (1.84 g, 28.9 mmol) was added and the mixture was stirred for 20 h at room temperature under an inert atmosphere. Solvents were removed in vacuo and azeotroped with toluene. The residue was dissolved in EtOAC, washed with saturated NaHCO3 then brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (eluant; 10% methanol:90% dichloromethane) to yield the title compound (3.0 g, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202858B2
Source datasetuspto-grants-2012_06
ORD IDord-30e1b01a1f9340e798e77cc3cde53b73
Source noteuspto-grants-2012_06