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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859198Generated: October 25, 2026

Sodium hydride → 3-[1-(2-Bromomethyl-benzyl)-indol-3-yl]-4-(1-methyl-indol-3-yl)-furan-2,5-dione

https://huagongshe.com/reaction/1859198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanto-Bis(bromomethyl)benzeneHCID 66665—
Reactant3-(1-Methyl-indol-3-yl)-4-(indol-3-yl)-furan-2,5-dioneHCID 14855714—
SolventDimethylformamideHCID 6228—
Product3-[1-(2-Bromomethyl-benzyl)-indol-3-yl]-4-(1-methyl-indol-3-yl)-furan-2,5-dioneHCID 2212326717.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 3-(indol-3-yl)-4-(1-methyl-indol-3-yl)-furan-2,5-dione (1.0 g, 3 mmol) and sodium hydride (154 mg, 3.5 mmol, 55-60% dispersion in oil) in dimethylformamide (20 mL) was stirred and cooled to 0° C., under a stream of nitrogen. After 35 min the solution was transferred to a dropping funnel and added slowly, over 40 min, to a solution of 1,2-bis-bromomethyl-benzene (3.8 g, 14.5 mmol) in dimethylformamide (6 mL). The resulting solution was stirred for 1 h at room temperature under a stream of nitrogen. The reaction was quenched by adding NaHCO3 (aq), and extracted with ethyl acetate. The organic phase was washed with several portions of water and dried (MgSO4). Evaporation followed by chromatography on silica (ethyl acetate:heptane, 3:7) afforded 270 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06153641
Source datasetuspto-grants-2000_11
ORD IDord-8157b277b9ec44f4b6e9471f085a20cd
Source noteuspto-grants-2000_11