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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408562Generated: October 26, 2026

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

https://huagongshe.com/reaction/1408562

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 5842414715%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxy-phenyl)-ethanone (19.45 g, 90.9 mmol), tetrahydro-2H-pyran-3-carbaldehyde (10 g, 90.9 mmol) and borax (34.6 g, 90.9 mmol) in ethanol (120 mL) and H2O (200 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-(tetrahydro-2H-pyran-3-yl)chroman-4-one (4 g, 15%). 1H-NMR (CDCl3): 1.30 (m, 2H), 1.48 (m, 5H), 1.64 (m, 4H), 1.94 (d, 2H), 6.86 (d, 1H), 7.51 (dd, 1H), 7.92 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-28c527dfb0314ce0b2e551e4437be269
Source noteuspto-grants-2014_12