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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Dibasic | HCID 24450 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-(4-Methoxyphenyl)-7-methyl-benzofuran | HCID 21071789 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-(4-Methoxy-phenyl)-benzofuran-7-carbaldehyde | HCID 21071790 | 50.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157491B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-af8f9388d9d640ec8835d587aa4c0212 |
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| Source note | uspto-grants-2007_01 |
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