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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637159Generated: October 25, 2026

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

https://huagongshe.com/reaction/1637159

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 numberUS06040306
Source datasetuspto-grants-2000_03
ORD IDord-c4ac2a5f0dc94c43a57d7d8459148877
Source noteuspto-grants-2000_03