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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462956Generated: October 31, 2026

1-(5-Chloro-2-hydroxyphenyl)-3-(4-chlorophenyl)-2-propen-1-one → 6-Chloro-2-(4-chlorophenyl)-2H-1-benzopyran

https://huagongshe.com/reaction/1462956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(5-Chloro-2-hydroxyphenyl)-3-(4-chlorophenyl)-2-propen-1-oneHCID 97894—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product6-Chloro-2-(4-chlorophenyl)-2H-1-benzopyranHCID 1620529355.5%

Reaction Steps

4,5'-Dichloro-2'-hydroxychalcone (7.32 g) was dissolved in ethanol (100 ml) and sodium borohydride (1.89 g) added in small portions. The reaction mixture was stirred for 1 hr at room temperature, evaporated to dryness, and diluted with water. The precipitated solid was filtered off, washed with water, and heated with acetic acid (100 ml) on the steam bath for 2 hr. The acetic acid was evaporated the residue dissolved in dichloromethane, and the solution washed sequentially with water, saturated sodium bicarbonate solution, and water, dried and evaporated. The residue was chromatographed on alumina, eluting with toluene, to give 4',6-dichloroflav-3-ene (3.84 g) as a colourless oil, identified by n.m.r. spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461907
Source datasetuspto-grants-1984_07
ORD IDord-45eb40cb01374ab890d9215ca8fb9483
Source noteuspto-grants-1984_07