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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940545Generated: October 30, 2026

Water → Benzofuran, 5-bromo-

https://huagongshe.com/reaction/1940545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
SolventDimethylformamideHCID 6228—
ProductBenzofuran, 5-bromo-HCID 9001530.5%

Reaction Conditions

Temperature150 °C

Reaction Steps

A solution of 4-bromophenol (17.3 g, 100 mmol) in dimethylformamide (40 ml) was treated with bromoacetaldehyde dimethyl acetal (16.9 g, 100 mmol) and potassium carbonate (13.8 g, 100 mmol) and heated at 150° C. for 16 h. The mixture was cooled, poured into water (500 ml) and extracted with diethyl ether (3×100 ml). The combined organic extracts were dried (MgSO4), concentrated, and filtered through a plug of silica gel eluting with 10% diethyl ether in hexane. The resulting oil (15 g) was added to a solution of polyphosphoric acid (~12 g) in toluene (100 mL) and heated at 80° C. for 16 h. The mixture was cooled and the toluene layer was decanted off and washed with saturated aqueous sodium hydrogen carbonate, dried (MgSO4), concentrated and the residue distilled to give 5-bromobenzofuran (6 g) as a colourless oil, bp. 98° C./1 mmHg; δH (DMSO-d6) 6.96 (1H, m, ArH), 7.45 (1H, m, ArH), 7.59 (1H, m, ArH), 7.91 (1H, m, ArH), and 8.05 (1H, m, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700809
Source datasetuspto-grants-1997_12
ORD IDord-c4ecce3b03ab46b887013a11c6cfea41
Source noteuspto-grants-1997_12