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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096407Generated: November 1, 2026

4-Fluorobenzaldehyde → 6-Bromo-2-(4-fluoro-phenyl)-chroman-4-one

https://huagongshe.com/reaction/2096407

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Bromo-2-(4-fluoro-phenyl)-chroman-4-oneHCID 5842402322.2%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxy-phenyl)-ethanone (30 g, 0.14 mol), 4-fluorobenzaldehyde (19.3 g, 0.14 mol) and borax (53.34 g, 0.14 mol) in ethanol (180 mL) and H2O (300 mL) was refluxed for one day. The reaction mixture was cooled, diluted with an equal volume of H2O and extracted with ethyl acetate. The organic layer was dried over anhydrous Na2SO4, filtered, and evaporated to give 6-bromo-2-(4-fluoro-phenyl)-chroman-4-one (10 g, 20%). 1H-NMR (CDCl3): 2.81 (dd, 1H), 2.99 (t, 1H), 5.49 (dd, 1H), 6.87 (d, 1H), 7.04 (t, 2H), 7.38 (t, 2H), 7.51 (dd, 1H), 7.94 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-3e6f44cb32344a899778c20c462cb6b0
Source noteuspto-grants-2013_05