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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23554Generated: October 29, 2026

Potassium Hydroxide → 2-(3-{[(Tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetic acid

https://huagongshe.com/reaction/23554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantTert-butyl 2-(3-{[(tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetateHCID 22574614—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(3-{[(Tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetic acidHCID 1554234232%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of tert-butyl 2-(3-{[(tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetate (1.14 g) in ethanol (10 ml) and water (10 ml) was added potassium hydroxide (0.22 g) and then the reaction mixture stirred at 70° C. for 5 hours. After the ethanol was removed under reduced pressure, to the residue was added saturated aqueous sodium hydrogen carbonate solution. The aqueous phase was washed with ethyl acetate, acidified with 10% hydrochloric acid and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, filtered and evaporated under reduced pressure. The precipitate was recrystallized with ethyl acetate and filtered off to give 2-(3-{[(tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetic acid (0.30 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852744B2
Source datasetuspto-grants-2005_02
ORD IDord-5659fba9de034669956957442858295b
Source noteuspto-grants-2005_02