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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57739Generated: October 29, 2026

Ammonia → (R)-diethyl 2-benzyloxycarbonylamino-2-carbamoylsuccinate

https://huagongshe.com/reaction/57739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantIsobutyl chloroformateHCID 62365—
Reactant(R)-1-ethyl hydrogen 3-benzyloxycarbonylamino-3-ethoxycarbonylsuccinateHCID 66725113—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product(R)-diethyl 2-benzyloxycarbonylamino-2-carbamoylsuccinateHCID 6672515184%

Reaction Steps

A solution of (R)-1-ethyl hydrogen 3-benzyloxycarbonylamino-3-ethoxycarbonylsuccinate (1.8 g) in THF (20 mL) was added with triethylamine (0.96 mL) and isobutyl chloroformate (0.84 mL, 0.87 g) in this order at −15° C. with stirring, and the mixture was stirred for 5 minutes. A solution of 25% aqueous ammonia (0.47 mL) was dropped into the reaction mixture at the same temperature. The reaction mixture was stirred at the same temperature for 1 hour, and then poured into diluted hydrochloric acid, the mixture was extracted with ethyl acetate, and the extract was 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 crystallized from ethyl acetate/n-hexane to obtain the title compound (1.51 g, yield: 84%) as colorless crystals. Optical rotation [α]D25 was −5.7° (c 0.52, ethanol) and optical purity was 96.1% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434737B2
Source datasetuspto-grants-2016_09
ORD IDord-e294c7aa81634a2daab12f0f49e89a88
Source noteuspto-grants-2016_09