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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714590Generated: October 31, 2026

Benzaldehyde → Chromanone

https://huagongshe.com/reaction/714590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantPyrrolidineHCID 31268—
Reactantalpha-HydroxyacetophenoneHCID 68490—
SolventMethanolHCID 887—
ProductChromanoneHCID 68110—

Reaction Conditions

Temperature50 °C

Reaction Steps

2-Hydroxyacetophenone compounds of structure XXXXI are treated with benzaldehyde compounds of structure XXXXII under suitable conditions to provide chroman-4-one compounds of structure XXXXIII. In some embodiments, 2-hydroxyacetophenone compounds of structure XXXXI are treated with benzaldehyde compounds of structure XXXXII, pyrrolidine, and methanol, with heating to about 50° C. for about 2 days to provide chroman-4-one compounds of structure XXXXIII. Chroman-4-one compounds of structure XXXXIII are then reacted tris(dibenzylideneacetone)dipalladium(0), tri-tert-butylphosphonium tetrafluoroborate, potassium bicarbonate, a suitable arylbromide, and 1,4-dioxane/water (4:1,) at about 110° C. to provide chroman-4-one compounds of structure XXXXIV. Chroman-4-one compounds of structure XXXXIV are then treated with methyl magnesium chloride in tetrahydrofuran at about 0° C., followed by 80% AcOH/H2O with warming to about 90° C. to provide compounds of structure XXXXV.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187460B2
Source datasetuspto-grants-2015_11
ORD IDord-8a0531dec7b44478bcb083e8297461e9
Source noteuspto-grants-2015_11