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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372162Generated: October 30, 2026

Potassium Phosphate, Dibasic → 5-(4-Methoxy-phenyl)-benzofuran-7-carbaldehyde

https://huagongshe.com/reaction/1372162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, DibasicHCID 24450—
ReactantN-bromobutanimideHCID 67184—
Reactant5-(4-Methoxyphenyl)-7-methyl-benzofuranHCID 21071789—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product5-(4-Methoxy-phenyl)-benzofuran-7-carbaldehydeHCID 2107179050.1%

Reaction Steps

To a solution of 5-(4-methoxyphenyl)-7-methyl-benzofuran (1.60 g, 2.83 g 1:1 ratio with 4-methoxy-biphenyl 6.72 mmol) in carbon tetrachloride (190 ml) was added NBS (1.32 g, 7.40 mmol) and AIBN (50 mg). The solution was brought to reflux for 2 h, cooled to room temperature, and the solids were filtered off. The solution was then concentrated and anhydrous CH3CN (80 ml) was added. Then potassium benzeneselenite (2.14 g, 9.41 mmol), and K2HPO4 (1.17 g, 6.72 mmol) were added and then reaction was heated to reflux for 1 h after which it was allowed to cool to room temperature. The solution was then passed through a silica plug and concentrated under high vacuum. Chromatography (100% CH2Cl2) afforded 850 mg (50%) product as a white solid: mp 94–95° C.; 1H NMR (300 MHz, DMSO-d6): δ 3.82 (3H, s), 7.08 (2H, d, J=8.8 Hz), 7.14 (1H, d, J=2.2 Hz), 7.71 (2H, d, J=8.8 Hz), 8.10 (1H, d, J=1.9 Hz), 8.21 (1H, d, J=2.2 Hz), 8.25 (1H, d, J=1.9 Hz), 10.37 (1H, s); MS (ESI) m/z 253 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157491B2
Source datasetuspto-grants-2007_01
ORD IDord-af8f9388d9d640ec8835d587aa4c0212
Source noteuspto-grants-2007_01