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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108575Generated: October 30, 2026

Iodoethane → tert-Butyl 4-ethyl-3-oxopiperazine-1-carboxylate

https://huagongshe.com/reaction/1108575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-ethyl-3-oxopiperazine-1-carboxylateHCID 1878391770.2%

Reaction Steps

1-tert-Butoxycarbonyl-3-oxopiperazine (7.5 g) was dissolved in dry DMF (250 ml) and potassium tert-butoxide (8.4 g) was added. The mixture was stirred at ambient temperature for 30 minutes, then iodoethane (3.3 ml) added, and stirring continued at the same temperature for 24 hours. A further equal portion of iodoethane was added and stirring continued for 24 hours. Solvent was evaporated, and the residue partitioned between ethyl acetate and water. The organic layer was washed with water, evaporated, and purified by chromatography on silica, using as eluant a gradient increasing in polarity from 0 to 25% isopropanol in iso-hexane. Relevant fractions were combined and evaporated to give 1-tert-butoxycarbonyl-4-ethyl-3-oxopiperazine (6.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069145
Source datasetuspto-grants-2000_05
ORD IDord-aa432de30c7e46eca6a4251d1934c76a
Source noteuspto-grants-2000_05