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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021218Generated: November 1, 2026

Cesium carbonate → Ethyl 1-[2-fluoro-3-(hydroxymethyl)phenyl]piperidine-4-carboxylate

https://huagongshe.com/reaction/1021218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantBinap, (A+-)-HCID 634876—
Reactant((3-Bromo-2-fluorobenzyl)oxy)(tert-butyl)dimethylsilaneHCID 86686195—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductEthyl 1-[2-fluoro-3-(hydroxymethyl)phenyl]piperidine-4-carboxylateHCID 6830890457.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under argon atmosphere, [(3-bromo-2-fluorobenzyl)oxy](tert-butyl)dimethylsilane (2 g) and ethyl piperidine-4-carboxylate (1.6 g) were mixed with toluene (30 ml), and Pd2(dba)3 (150 mg), BINAP (300 mg), and cesium carbonate (3.2 g) were added thereto, followed by stirring at 100° C. for 1 hour. The reaction mixture was cooled to room temperature, and EtOAc was added thereto, followed by filtration using Celite as a filtration adjuvant. The filtrate was concentrated under reduced pressure, the residue was then mixed with THF (30 ml), and a 1 M TBAF/THF solution (12 ml) was added thereto, followed by stirring at room temperature for 1 hour. To the reaction mixture were added EtOAc and water, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain ethyl 1-[2-fluoro-3-(hydroxymethyl)phenyl]piperidine-4-carboxylate (1.02 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-2230caff0e68418180964caf535523ae
Source noteuspto-grants-2014_05