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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096400Generated: October 31, 2026

5'-Bromo-2'-hydroxyacetophenone → 6-Bromo-2-(3-fluorophenyl)chroman-4-one

https://huagongshe.com/reaction/2096400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
Reactant2,3-DifluorobenzaldehydeHCID 137664—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-Bromo-2-(3-fluorophenyl)chroman-4-oneHCID 5842406815%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxy-phenyl)-ethanone (22.6 g, 0.11 mol), 2,3-difluoro-benzaldehyde (15 g, 0.11 mol) and borax (40.2 g, 0.11 mol) in ethanol (140 mL) and H2O (234 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 (5.3 g, 15%). 1H-NMR (CDCl3): 2.95 (d, 1H), 3.05 (t, 3H), 5.75 (d, 1H), 6.97 (d, 1H), 7.20 (m, 2H), 7.35 (m, 1H), 7.60 (d, 1H), 8.05 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-f560d58ae3ce4492a46d0485572cec4f
Source noteuspto-grants-2013_05