HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57735Generated: October 24, 2026
Hydrochloric Acid → Diethyl 2-benzyloxycarbonylamino-2-ethoxycarbonylsuccinate
https://huagongshe.com/en/reaction/57735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diethyl 2-(benzyloxycarbonylamino)malonate | HCID 259787 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-benzyloxycarbonylamino-2-ethoxycarbonylsuccinate | HCID 66725114 | 86.1% |
Reaction Steps
A suspension of diethyl 2-benzyloxycarbonylaminomalonate (5.0 g), potassium carbonate (2.7 g), potassium iodide (0.27 g), and ethyl 2-chloroacetate (2.6 g) in DMF (50 mL) was stirred at 50° C. for 1 hour. 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 crystallized from ethyl acetate/n-hexane to obtain the title compound (5.5 g, yield: 86%) as colorless crystals.
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-3894c10f70494b50b9b7b28ab01b5f7e |
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| Source note | uspto-grants-2016_09 |
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