HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988185Generated: November 4, 2026
Benzoyl Peroxide → 7-(bromomethyl)-4-(4-fluorophenyl)-2H-chromen-2-one
https://huagongshe.com/reaction/1988185
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-(4-fluorophenyl)-7-methyl-2H-chromen-2-one | HCID 57729246 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(bromomethyl)-4-(4-fluorophenyl)-2H-chromen-2-one | HCID 19426963 | — |
Reaction Steps
A mixture of 4-(4-fluorophenyl)-7-methyl-2H-chromen-2-one (24.0, 94.3 mmol), NBS (18.5 g, 103.8 mmol) and benzoyl peroxide (1.14 g, 4.72 mmol) in 470 mL of CCl4 was brought to reflux. The solution was left overnight at reflux and then filtered hot. Once cooled to rt the solvent was removed, the compound was dissolved in CH2Cl2 and a purification was done with a small pad of silica gel using hexane-EtOAc (8/2) to (1/1). The solvent was removed and the solid triturated with hexane-EtOAc and filtered to give the title compound. The remaining solvent was removed to give additional compound contaminated with some starting material and dibromo compound. 1H NMR (400 MHz, acetone-d6): δ 7.67 (2H, m), 7.55 (1H, s), 7.50 (1H, d), 7.40 (3H, m), 6.40 (1H, s) and 4.75 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07553973B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-286febfb7e924532958035e060139d3c |
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| Source note | uspto-grants-2009_06 |
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