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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897564Generated: October 30, 2026

Piperidine → HCID 57659744, compound

https://huagongshe.com/reaction/1897564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 12026771HCID 12026771—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 57659744HCID 5765974415%

Reaction Steps

A solution of methyl 5-tert-butyl-2-(bromomethyl)furan-3-carboxylate (0.28 g, 1.0 mmol) and piperidine (99 μL, 1 mmol) in acetone (5 mL) was stirred at room temperature 3 days. The mixture was diluted with water and extracted with EtOAc. The organic extracts were washed with water, dried over Na2SO4, and concentrated under vacuum. The residue was purified by silica gel chromatography (0%-50% EtOAc-hexanes) to obtain methyl 5-tert-butyl-2-((piperidin-1-yl)methyl)furan-3-carboxylate (41 mg, 15% yield). LC/MS: m/z 280.3 (M+H)+ at 2.10 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519137B2
Source datasetuspto-grants-2013_08
ORD IDord-b2f64f00c2a741f69c2b60a3f76d679b
Source noteuspto-grants-2013_08