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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096505Generated: November 3, 2026

5'-Bromo-2'-hydroxyacetophenone → HCID 58424670, compound

https://huagongshe.com/reaction/2096505

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
ReactantTetrahydro-2H-pyran-4-carboxaldehydeHCID 9964078—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 58424670HCID 5842467020%

Reaction Steps

To a stirred solution of 1-(5-bromo-2-hydroxyphenyl)ethanone (943.9 mg, 4.39 mmol) in EtOH (5.6 mL) and H2O (9.4 mL) was added tetrahydro-2H-pyran-4-carbaldehyde (500 mg, 4.39 mmol) and borax (1.67 g, 4.39 mmol). The mixture was refluxed overnight. Then the mixture was filtered and the filtrate was concentrated in vacuo. The resulting residue was dissolved in CR2Cl2 and filtrated. The filtrate was concentrated in vacuo to give the crude product, which was purified by column chromatography to give 6-bromo-2-(tetrahydro-2H-pyran-4-yl)chroman-4-one (270 mg, 20%). 1H-NMR (CDCl3, 400 MHz): 1.54 (m, 2H), 1.78 (m, 1H), 1.95 (m, 1H), 2.75 (m, 2H), 3.44 (m, 3H), 4.09 (m, 2H), 4.15 (m, 1H), 6.89 (m, 1H), 7.56 (m, 1H), 8.01 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-aa7fcc242797468189b9d6e979fed8f0
Source noteuspto-grants-2013_05