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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931691Generated: October 30, 2026

Bromide ion → HCID 85764348, compound

https://huagongshe.com/reaction/931691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantDiethyl MalonateHCID 7761—
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)benzophenoneHCID 122951—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 85764348HCID 8576434886%

Reaction Conditions

Temperature0 °C

Reaction Steps

60% mineral oil suspension of sodium hydride (1.454 g; 36.3 mmol) was added into anhydrous DMF (50 mL) under nitrogen at 0° C. Diethyl malonate (5.82 g; 36.3 mmol) was added to the stirred suspension over 10 min and the mixture was then stirred rapidly at 0° C. until a clear pale yellow solution was obtained. 4-(bromomethyl)benzophenone (5.00 g; 18.2 mmol) in DMF (15 mL) was added dropwise over 5 min and the reaction mixture was stirred for 16 h at ambient temperature. Complete conversion of the starting bromide was confirmed by TLC. The reaction was diluted with water (400 mL) and extracted with dichloromethane (3×50 mL). The organic phase was separated, dried and evaporated to an oily residue. Chromatography on silicagel (eluent hexane/2-butanone 10:1→5:1) provided the desired 1,3-diethyl 2-[(4-benzoylphenyl)methyl]propanedioate (5.47 g; 86%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296835B2
Source datasetuspto-grants-2016_03
ORD IDord-4ba7865f2a3a4e0fa87997cd7a2d1951
Source noteuspto-grants-2016_03