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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522871Generated: October 30, 2026

HCID 12364533, compound → HCID 12364536, compound

https://huagongshe.com/reaction/522871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12364533HCID 12364533—
SolventHydrochloric AcidHCID 313—
ProductHCID 12364536HCID 1236453666.66%

Reaction Steps

A solution of 1-benzyl-3-(2-oxo-2-phenylethyl)piperidin-4-one (4.0 g, 0.0129 mol) in conc. HCl (50 mL) was heated at reflux for 3 h. After consumption of the starting material as determined by TLC, the reaction mixture was cooled down to RT and made alkaline by the addition of NH4OH, then extracted with diethyl ether. The organics were dried over Na2SO4 and concentrated to afford 5-benzyl-2-phenyl-4,5,6,7-tetrahydrofuro[3,2-c]pyridine (2.0 g, 66.66%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-fa44da748c9a40c9b8ec38c2965453e6
Source noteuspto-grants-2016_05