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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408688Generated: October 26, 2026

5'-Bromo-2'-hydroxyacetophenone → 6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one

https://huagongshe.com/reaction/1408688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
ReactantOxane-3-carbaldehydeHCID 10129928—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-oneHCID 5842414720%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxyphenyl)ethanone (39 g, 181.8 mmol), tetrahydro-2H-pyran-3-carbaldehyde (20 g, 181.8 mmol) and borax (69.3 g, 181.8 mmol) in ethanol (240 mL) and H2O (400 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 concentrated in vacuo to give 6-bromo-2-(tetrahydro-2H-pyran-3-yl)chroman-4-one (10 g, 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-2fb87bf457da4e13973f024e09ca42e9
Source noteuspto-grants-2014_12