HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666897Generated: November 1, 2026
Benzoyl Peroxide → 4-Fluoro-3-phenoxybenzaldehyde
https://huagongshe.com/reaction/1666897
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 1-Fluoro-4-methyl-2-phenoxybenzene | HCID 14257298 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-Fluoro-3-phenoxybenzaldehyde | HCID 110068 | 8.5% |
Reaction Steps
Combine 4-fluoro-1-methyl-3-phenoxybenzene (2.43 g, 12.0 mmol), N-bromosuccinimide (4.92 g, 27.6 mmol), benzoyl peroxide (408 mg, 1.68 mmol), and carbon tetrachloride (55 mL). Heat the mixture at reflux temperature for 6.5 h and cool to 0° C. for 64 h. Filter the solids and concentrate the filtrate. Dissolve the residue in chloroform and wash with ice cold sodium carbonate solution. Dry the chloroform solution over sodium sulfate, filter and concentrate under reduced pressure. Dissolve the residue in acetonitrile (50 mL) and add 4-methylmorpholine-4-oxide (4.6 g, 39.1 mmol) and powdered 4 Å sieves (200 mg). Stir at ambient temperature for 20 h, filter and concentrate. Purify by silica gel chromatography (5%, 30% ethyl acetate/hexanes) to give 220 mg (8%) of the title compound: MS (m/e): 216 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044090B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-e42d67a88943494da449cce1208df126 |
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| Source note | uspto-grants-2011_10 |
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