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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099909Generated: October 26, 2026

N-Boc-2-Maleimidoethylamine → N-(2-Aminoethyl)maleimide

https://huagongshe.com/reaction/2099909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Boc-2-MaleimidoethylamineHCID 4176840—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductN-(2-Aminoethyl)maleimideHCID 2778791100%

Reaction Conditions

Temperature0 °C

Reaction Steps

(2-Maleimido)ethylcarbamic acid tert-butyl ester (48 mg, 0.2 mmol) was dissolved in a mixed solvent of trifluoroacetic acid and dichloromethane (30:70, 5 ml), followed by stirring at 0° C. for 2 hours, and then the reaction solution was concentrated. The thus obtained residue was dissolved in dichloromethane (20 ml), and a saturated aqueous sodium hydrogencarbonate solution (10 ml) was added thereto to separate the layers. The organic layer was dried over potassium hydrogencarbonate and filtered. The solvent was evaporated under reduced pressure to give 1-(2-aminoethyl)-3-pyrroline-2,5-dione (28 mg, 0.2 mmol, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569706B2
Source datasetuspto-grants-2009_08
ORD IDord-1e65fa069d384eed805152a5d6d2aeb3
Source noteuspto-grants-2009_08