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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57745Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/57745

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 numberUS09434737B2
Source datasetuspto-grants-2016_09
ORD IDord-602dde33759e487e961a51b22824aeaa
Source noteuspto-grants-2016_09