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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Tert-butyl 2-(3-{[(tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetate | HCID 22574614 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-{[(Tert-butyl)oxycarbonyl]methyl}-2-oxoimidazolidinyl)acetic acid | HCID 15542342 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852744B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-5659fba9de034669956957442858295b |
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| Source note | uspto-grants-2005_02 |
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