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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096439Generated: October 29, 2026

3-Fluorobenzaldehyde → 6-Bromo-2-(3-fluorophenyl)chroman-4-one

https://huagongshe.com/reaction/2096439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzaldehydeHCID 68009—
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Bromo-2-(3-fluorophenyl)chroman-4-oneHCID 5842406836.9%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxy-phenyl)-ethanone (15 g, 0.07 mol), 3-fluorobenzaldehyde (8.7 g, 0.07 mol) and borax (26.7 g, 0.07 mol) in ethanol (90 mL) and H2O (150 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-(3-fluorophenyl)chroman-4-one (8.3 g, 3.7%). 1H-NMR (CDCl3): 2.93 (d, 1H), 3.03 (m, 1H), 5.47 (d, 1H), 7.06 (d, 1H), 7.11 (m, 1H), 7.22 (m, 2H), 7.40 (m, 1H), 7.57 (d, 1H), 8.04 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-0ee9580a85144962ad224a91ccd30e8e
Source noteuspto-grants-2013_05