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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971949Generated: October 30, 2026

Selectfluor → Benzyl 3-fluoro-4-oxopiperidine-1-carboxylate

https://huagongshe.com/reaction/1971949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSelectfluorHCID 2724933—
ReactantBenzyl 4-((trimethylsilyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylateHCID 57502431—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductBenzyl 3-fluoro-4-oxopiperidine-1-carboxylateHCID 4260925312.2%

Reaction Steps

To a stirred solution of 4-trimethylsilanyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester (5 g, 16.4 mmol) in acetonitrile at 0° C. was added 1-(chloromethyl)-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane ditetrafluoroborate (6.4 g, 18 mmol). The solution was stirred overnight at room temperature, concentrated, diluted with EtOAc and washed with water. The organics were dried over sodium sulfate, filtered, concentrated, and purified by column chromatography using 40-60% EtOAc in hexanes to give 3-fluoro-4-oxo-piperidine-1-carboxylic acid benzyl ester (3.1 g) To a stirred solution of 3-fluoro-4-oxo-piperidine-1-carboxylic acid benzyl ester (500 mg, 2 mmol) in ethanol (6 mL) was added sodium borohydride (100 mg, 2.6 mmol). After 0.5 hr, the mixture was concentrated, diluted with EtOAc and washed with water. The organics were dried over sodium sulfate, filtered, concentrated, and purified by column chromatography using 40-70% EtOAc in hexanes to give (±)-trans-3-fluoro-4-hydroxy-piperidine-1-carboxylic acid benzyl ester (120 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431575B2
Source datasetuspto-grants-2013_04
ORD IDord-2f23163b51f2419eb763b0b36bc43910
Source noteuspto-grants-2013_04