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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401943Generated: November 1, 2026

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

https://huagongshe.com/reaction/401943

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 numberUS08741900B2
Source datasetuspto-grants-2014_06
ORD IDord-26d5049b879c4584b956ec84ac771747
Source noteuspto-grants-2014_06