HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57746Generated: October 24, 2026
Hydrochloric Acid → Diethyl 2-t-butyloxycarbonylamino-2-ethoxycarbonylsuccinate
https://huagongshe.com/en/reaction/57746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl 2-((tert-butoxycarbonyl)amino)malonate | HCID 382219 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-t-butyloxycarbonylamino-2-ethoxycarbonylsuccinate | HCID 86661708 | 86.8% |
Reaction Steps
A suspension of diethyl 2-t-butyloxycarbonylaminomalonate (5.0 g), potassium carbonate (3.0 g), and ethyl 2-bromoacetate (3.9 g) in DMF (20 mL) was stirred at 50° C. for 4 hours. The reaction mixture was cooled, and then poured into diluted hydrochloric acid, the mixture was extracted with ethyl acetate, and the extract was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography, and then purification was performed with n-hexane/ethyl acetate (5:1), to obtain the title compound (5.7 g, yield: 79%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434737B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-b3b222236c0b4483b363d013ccd349df |
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| Source note | uspto-grants-2016_09 |
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