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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293437Generated: October 30, 2026

Benzyl Bromide → 4-Benzyloxy dibenzo[b,d]furan-1-carbaldehyde

https://huagongshe.com/reaction/1293437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy dibenzo[b,d]furan-1-carbaldehydeHCID 44225196—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy dibenzo[b,d]furan-1-carbaldehydeHCID 8596705890.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

Intermediate 19 (1 gm, 5.10 mmol) was dissolved in dry DMF (10 ml). Anhydrous potassium carbonate (1.05 gm, 7.65 mmol) was added to the above solution and was stirred for 10 min. at 80° C. To this was added benzyl bromide (0.87 gm, 5.10 mmol) and the reaction mixture was stirred for 2 h. The reaction mixture was cooled to room temperature and diluted with water (100 ml) and extracted with ethyl acetate (3×50 ml). The organic extract was washed with water (50 ml) and brine solution (25 ml) and dried over anhydrous sodium sulfate. Removal of solvent gave the product as a brown solid (1.4 gm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238725B2
Source datasetuspto-grants-2007_07
ORD IDord-3d637748b5774261b7e6761ed5ec0bd7
Source noteuspto-grants-2007_07