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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371148Generated: October 31, 2026

Iodoethane → (2R)-1-(tert-butoxycarbonyl)-4-ethylpiperazine-2-carboxylic acid

https://huagongshe.com/reaction/2371148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium CarbonateHCID 10340—
Reactant(2R)-1-(tert-Butoxycarbonyl)piperazine-2-carboxylic acidHCID 24820285—
SolventEthanolHCID 702—
Product(2R)-1-(tert-butoxycarbonyl)-4-ethylpiperazine-2-carboxylic acidHCID 59846012—

Reaction Steps

To (2R)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid (1.406 g) and Na2CO3 (2.59 g) was added dry EtOH (28 ml) then ethyl iodide (0.54 ml) and the mixture heated at reflux for 18 h under argon. The solvent was then removed under reduced pressure and 5% MeOH/DCM (40 ml) was added and stirred for 1 hour in a sealed flask. The solution was filtered and washed with dichloromethane (2×10 mL). The filtrate was then placed directly onto a 120 g-silica cartridge and was purified using eluent 10-70% MeOH/DCM. After evaporation, the product was isolated as a white foam (1.00 g), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710224B2
Source datasetuspto-grants-2014_04
ORD IDord-96b2d6ecc74443ad8ec9e7a7cf682d34
Source noteuspto-grants-2014_04