HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57742Generated: October 24, 2026
Hydrochloric Acid → Diethyl 2-benzyloxycarbonylamino-2-(methoxycarbonylmethyl)malonate
https://huagongshe.com/en/reaction/57742
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Diethyl 2-(benzyloxycarbonylamino)malonate | HCID 259787 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Diethyl 2-benzyloxycarbonylamino-2-(methoxycarbonylmethyl)malonate | HCID 66725236 | 95.2% |
Reaction Steps
A suspension of diethyl 2-benzyloxycarbonylaminomalonate (3.0 g), potassium carbonate (1.6 g), potassium iodide (0.19 g), and methyl 2-bromoacetate (1.9 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 subjected to silica gel column chromatography, in which elution was performed with n-hexane/ethyl acetate (4:1) for purification, and then crystallized from ethyl acetate/n-hexane to obtain the title compound (3.52 g, yield: 95%) 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-995c581b90244a03a1e384a2adaad932 |
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| Source note | uspto-grants-2016_09 |
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