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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509181Generated: October 31, 2026

Piperidine → Ethyl alpha-phenyl-1-piperidineacetate

https://huagongshe.com/reaction/509181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantEthyl bromophenylacetateHCID 97780—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl alpha-phenyl-1-piperidineacetateHCID 20213534.1%

Reaction Steps

To a solution of ethyl 2-bromo-2-phenylacetate 21 (1.50 g, 6.17 mmol) in THF (10 mL) at room temperature was added piperidine (0.641 mL, 6.48 mmol) and TEA (1.72 mL, 12.34 mmol) and the reaction mixture was stirred for 3 h then diluted with brine and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated. The crude material was purified by silica gel column chromatography with gradient of ethyl acetate (0-50%) in hexane to afford 22 as a colorless viscous oil (520 mg, 34%). LRMS (ESI): (calc) 247.3 (found) 248.3 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096565B2
Source datasetuspto-grants-2015_08
ORD IDord-54972073c7574747a226b04061e42352
Source noteuspto-grants-2015_08