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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666897Generated: November 1, 2026

Benzoyl Peroxide → 4-Fluoro-3-phenoxybenzaldehyde

https://huagongshe.com/reaction/1666897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl morpholine oxideHCID 82029—
Reactant1-Fluoro-4-methyl-2-phenoxybenzeneHCID 14257298—
SolventCarbon TetrachlorideHCID 5943—
Product4-Fluoro-3-phenoxybenzaldehydeHCID 1100688.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044090B2
Source datasetuspto-grants-2011_10
ORD IDord-e42d67a88943494da449cce1208df126
Source noteuspto-grants-2011_10