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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471347Generated: November 1, 2026

Hydrochloric Acid → Diethyl 2-benzyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate

https://huagongshe.com/reaction/471347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl bromoacetateHCID 62576—
ReactantDiethyl 2-(benzyloxycarbonylamino)malonateHCID 259787—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-benzyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonateHCID 6672516399%

Reaction Steps

A solution of diethyl 2-benzyloxycarbonylaminomalonate (30 g) in anhydrous DMF (100 mL) was added portionwise with sodium hydride (60%, 4.27 g) with ice cooling and stirring, then the mixture was stirred at room temperature for 30 minutes, and then added with benzyl 2-bromoacetate (28.9 g), and the mixture was stirred overnight. The reaction mixture was 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, and then purification was performed with n-hexane/ethyl acetate (4:1), to obtain the title compound (43.9 g, yield: 99%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633001B2
Source datasetuspto-grants-2014_01
ORD IDord-2d73af51113c436dbf6e9c021c2bb7b1
Source noteuspto-grants-2014_01