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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513697Generated: October 29, 2026

1,2-Dibromoethane → HCID 68183475, compound

https://huagongshe.com/reaction/513697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantMagnesiumHCID 5462224—
Reactant8-Nitro-7-quinolinecarboxaldehydeHCID 11769554—
Reactant2-(5-Bromo-2-fluorophenyl)-1,3-dioxolaneHCID 18455585—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68183475HCID 6818347574%

Reaction Steps

Magnesium (983 mg, 40.5 mmol) was suspended in anhydrous THF (30 ml). 1,2-dibromoethane (0.17 ml, 2.02 mmol) was added and the solution was stirred at room temperature for 20 min. 2-(5-bromo-2-fluoro-phenyl)-[1,3]dioxolane 417 (3.2 g, 12.95 mmol) was added dropwise and the mixture was heated at 40° C. for 2 h. The mixture was allowed to cool to room temperature. The Grignard reagent (0.43M; 28.6 ml) was added to a suspension of 8-nitroquinoline-7-carbaldehyde 204 (2.5 g, 12.4 mmol) in dry THF (30 ml) at 0° C. under a nitrogen atmosphere. The mixture was stirred at room temperature for 30 min. The mixture was quenched with sat. NH4Cl (10 ml) and the aqueous phase was extracted with EtOAc (20 ml). The organic phase was washed with brine (10 ml), dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with heptane/EtOAc (50:50) as the eluent to give the title compound (3.39 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102688B2
Source datasetuspto-grants-2015_08
ORD IDord-6dadb1431f37459f8b87789e4d0ac191
Source noteuspto-grants-2015_08