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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-diethyl 2-t-butyloxycarbonylamino-2-carbamoylsuccinateHCID 86661710—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(R)-2-t-butyloxycarbonylamino-2-ethoxycarbonylsuccinimideHCID 6672514388.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434737B2
Source datasetuspto-grants-2016_09
ORD IDord-d091c5fb010541d79dd26b5cf18c724f
Source noteuspto-grants-2016_09