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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49794Generated: October 26, 2026

Ethyl Acetate → O-tert-butyl N-(4-fluorobenzyl)-N-(1-acetylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/49794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzyl bromideHCID 68021—
Reactanttert-Butyl (1-acetylpiperidin-4-yl)carbamateHCID 22741830—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductO-tert-butyl N-(4-fluorobenzyl)-N-(1-acetylpiperidin-4-yl)carbamateHCID 9841338—

Reaction Steps

To a solution of O-tert-butyl (1-acetylpiperidin-4-yl)carbamate (0.97 g) in N,N-dimethylformamide (10 ml) was added 60% sodium hydride (0.18 g) at ambient temperature. After stirring for 40 minutes, 4-fluorobenzyl bromide (0.6 ml) was added to the reaction mixture. After additional stirring for 4 hours, the reaction mixture was poured into a mixture of ethyl acetate (50 ml) and water (10 ml). An organic phase was separated and washed with water and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. A residue was purified by column chromatography (silica gel 100 ml, toluene:ethyl acetate=1:1 to 1:2). After crystallization from diisopropyl ether and n-hexane, O-tert-butyl N-(4-fluorobenzyl)-N-(1-acetylpiperidin-4-yl)carbamate (922 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-110ac8c91a2f40a1a3df0e7c232ab79c
Source noteuspto-grants-2004_03