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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250162Generated: October 26, 2026

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

https://huagongshe.com/reaction/1250162

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 chromatoraphed (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 numberUS06337329B1
Source datasetuspto-grants-2002_01
ORD IDord-68b36bf69e84494c97c0516d9a997d29
Source noteuspto-grants-2002_01