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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408574Generated: October 31, 2026

2-Thiophenecarboxaldehyde → HCID 10709982, compound

https://huagongshe.com/reaction/1408574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
Reactant5'-Bromo-2'-hydroxyacetophenoneHCID 95991—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 10709982HCID 1070998255.6%

Reaction Steps

A mixture of 1-(5-bromo-2-hydroxy-phenyl)-ethanone (20 g, 0.093 mol), thiophene-2-carbaldehyde (10.46 g, 0.093 mol) and borax (35.4 g, 0.093 mol) 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-thiophen-2-yl-chroman-4-one (16 g, 50%). 1H-NMR (CDCl3): 3.01 (m, 1H), 3.10 (m, 1H), 5.75 (dd, 1H), 6.94 (d, 1H), 7.02 (t, 1H), 7.05 (d, 1H), 7.32 (d, 1H), 7.54 (dd, 1H), 8.00 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921359B2
Source datasetuspto-grants-2014_12
ORD IDord-ecd2d6c09c60423eb9446cbc8a3c5cbd
Source noteuspto-grants-2014_12