HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57749Generated: October 28, 2026
Hydrochloric Acid → (R)-2-t-butyloxycarbonylamino-2-ethoxycarbonylsuccinimide
https://huagongshe.com/reaction/57749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (R)-diethyl 2-t-butyloxycarbonylamino-2-carbamoylsuccinate | HCID 86661710 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-2-t-butyloxycarbonylamino-2-ethoxycarbonylsuccinimide | HCID 66725143 | 88.5% |
Reaction Steps
(R)-diethyl 2-t-butyloxycarbonylamino-2-carbamoylsuccinate (590 mg) obtained in Example 15 was dissolved in acetone (6 mL) and water (6 mL), the solution was added with potassium carbonate (295 mg), the mixture was stirred for 6 hours, 1 mol/L hydrochloric acid was poured to the mixture, and the mixture was extracted with ethyl acetate. 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 (1:1) for purification, and then recrystallized from ethyl acetate/n-hexane to obtain the title compound (450 mg, yield: 88%) as colorless crystals. Optical rotation [α]D25 was −39.1° (c 0.50, ethanol).
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-d091c5fb010541d79dd26b5cf18c724f |
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| Source note | uspto-grants-2016_09 |
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