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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112762Generated: November 1, 2026

Hydrochloric Acid → HCID 23079679, compound

https://huagongshe.com/reaction/2112762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23079679HCID 23079679—

Reaction Steps

Powdered zinc (2.82 g, 0.043 mol) was suspended in tetrahydrofuran (50.0 mL) under flow of argon gas, and the suspension was mixed with ethyl bromodifluoroacetate (7.31 g, 0.036 mol) at room temperature, followed by stirring under reflux for five minutes. The mixture was further mixed with a solution of tert-butyl 4-oxopiperidinecarboxylate in tetrahydrofuran (3.00 mol/L, 10.0 mL, 0.030 mol), followed by stirring under reflux for two hours. After checking the completion of the reaction by thin layer chromatography, the reaction mixture was mixed with ethyl acetate and diluted hydrochloric acid (1.00 mol/L), followed by separation. The organic layer was sequentially washed with a saturated aqueous sodium bicarbonate solution and brine, was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane: chloroform=1:9) and thereby yielded tert-butyl 4-(ethoxycarbonyldifluoromethyl)-4-hydroxy-piperidinecarboxylate (7.39 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524852B2
Source datasetuspto-grants-2009_04
ORD IDord-feec1d76fd594d4d87e7e01ae0c11ce3
Source noteuspto-grants-2009_04