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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408594Generated: November 2, 2026

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

https://huagongshe.com/reaction/1408594

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-fluoro-benzaldehy-de (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 numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-2c4a4ac39442432fb9af2014a8a72f22
Source noteuspto-grants-2014_12