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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
ReactantDiethyl 2-(benzyloxycarbonylamino)malonateHCID 259787—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-benzyloxycarbonylamino-2-(methoxycarbonylmethyl)malonateHCID 6672523695.2%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434737B2
Source datasetuspto-grants-2016_09
ORD IDord-995c581b90244a03a1e384a2adaad932
Source noteuspto-grants-2016_09