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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582862Generated: October 25, 2026

2-Fluoroethyl p-Toluenesulfonate → 1-Tert-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine

https://huagongshe.com/reaction/1582862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoroethyl p-ToluenesulfonateHCID 256019—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product1-Tert-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazineHCID 22716468—

Reaction Steps

1-t-Butoxycarbonyl-3-oxopiperazine (21.6 g) is dissolved in dry DMF (500 ml) and potassium t-butoxide (24.2 g) is added. The mixture is stirred at 20-25° for 30 minutes, then 1-(4-methylphenylsulfonyloxy)-2-fluoroethane (J. Med. Chem., 23(9), 985-90 (1980), 25.9 g) is added and stirring continued at the same temperature for 24 hours. The solvent is removed and the residue partitioned between ethyl acetate and water. The organic phase is washed with water and concentrated. The residue is dissolved in isopropanol and diluted with iso-hexane forming a precipitate which is removed by filtration. The mixture is chromatographed (silica; eluting with a gradient increasing in polarity from 0 to 50% isopropanol in iso-hexane) to give 1-t-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06740652B2
Source datasetuspto-grants-2004_05
ORD IDord-edc0064bb7804bc5a0816ac99c51519e
Source noteuspto-grants-2004_05