Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915892Generated: October 30, 2026

Ethyl fluoroacetate → Tert-butyl [1-(fluoroacetyl)piperidin-4-yl]carbamate

https://huagongshe.com/reaction/915892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl fluoroacetateHCID 9988—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Solvent2,2,2-TrifluoroethanolHCID 6409—
ProductTert-butyl [1-(fluoroacetyl)piperidin-4-yl]carbamateHCID 5895985953.1%

Reaction Steps

A solution of 500 mg of tert-butyl piperidin-4-ylcarbamate and 345 mg of ethyl fluoroacetate in 1 ml of trifluoroethanol was heated under reflux for 8 hours. The reaction mixture was concentrated under reduced pressure, and 1 M hydrochloric acid was added to the resulting residue. Then, this was extracted with EtOAc, and the organic layer was washed with aqueous saturated sodium hydrogencarbonate and brine. This was then dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting residue was purified with silica gel column chromatography (eluent: chloroform to chloroform/methanol=30/1) to obtain 345 mg of tert-butyl [1-(fluoroacetyl)piperidin-4-yl]carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268150B2
Source datasetuspto-grants-2007_09
ORD IDord-eb8c7975127e446cb5bbc0ccf744fa09
Source noteuspto-grants-2007_09