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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505705Generated: October 29, 2026

Piperidine → HCID 66722872, compound

https://huagongshe.com/reaction/505705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTetrahydro-2H-pyran-4-carboxaldehydeHCID 9964078—
ReactantMethyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylateHCID 15309116—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 66722872HCID 6672287249.4%

Reaction Steps

A solution of methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate (2.9 mmol), tetrahydro-pyran-4-carbaldehyde (3.2 mmol), and piperidine (3.2 mmol) in 6 mL of methanol was heated to 65° C. overnight. The cooled mixture was diluted with ethyl acetate, washed with water and brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel, eluting with ethyl acetate in hexane from 10% to 40%, to give 430 mg of the desired product. ES-MS m/z 301 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781428B2
Source datasetuspto-grants-2010_08
ORD IDord-11a7dbd172134b8f9c2ff50c8442dd79
Source noteuspto-grants-2010_08