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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18181Generated: October 25, 2026

Sodium Carbonate → 3-Benzyl-7-bromo-5-methyl-benzofuran

https://huagongshe.com/reaction/18181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantSodium FormateHCID 2723810—
Reactant1-Bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzeneHCID 68585603—
CatalystTetrabutylammonium ChlorideHCID 70681—
CatalystBis(acetonitrile)dichloropalladiumHCID 6093782—
SolventDimethylformamideHCID 6228—
Product3-Benzyl-7-bromo-5-methyl-benzofuranHCID 5934492952.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

1-Bromo-3-iodo-5-methyl-2-(3-phenylallyloxy)-benzene (10.86 g, 25 mmol), tetrabutylammonium chloride (7.65 gm, 27.5 mmol), sodium carbonate (6.62 g, 62.46 mmol), sodium formate (1.7 g, 25 mmol), and bis(acetonitrile)dichloropalladium(II) (0.467 g, 1.8 mmol) was added to 50 ml DMF. The mixture was degassed and heated under nitrogen at 80° C. for 105 minutes, then cooled to room temperature. Water was added and the mixture was extracted with a hexanes/ethyl acetate (1:1) mixture. The solution was dried onto 20 gm silica gel, the silica gel was layered over 100 gm silica gel in a fritted funnel and eluted with four 400 ml portions of hexanes. The hexanes was removed under reduced pressure to give 3-benzyl-7-bromo-5-methyl-benzofuran (3.97 g, 52% yield). MS: (M+H)+ 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741326B2
Source datasetuspto-grants-2010_06
ORD IDord-7ac7c6a36b2d43f6bce03c300bbc3b33
Source noteuspto-grants-2010_06