Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905083Generated: October 29, 2026

Ethyl bromoacetate → ethyl {[5-chloro-3-(2-methylphenyl)-4-oxo-4H-1-benzopyran-7-yl]oxy}acetate

https://huagongshe.com/reaction/1905083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 14254481HCID 14254481—
SolventAcetoneHCID 180—
Productethyl {[5-chloro-3-(2-methylphenyl)-4-oxo-4H-1-benzopyran-7-yl]oxy}acetateHCID 1425450389.1%

Reaction Steps

In 1 l of acetone was suspended 114 g of 5-chloro-7-hydroxy-3-(2-methylphenyl)-4-oxo-4H-1-benzopyran, and 60.4 g of anhydrous potassium carbonate and 73.0 g of ethyl bromoacetate were added thereto, followed by refluxing for 1.5 hours. After cooling, the insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. Recrystallization of the residue from ethanol gave 132 g of the entitled compound having a melting point of 122° to 123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841076
Source datasetuspto-grants-1989_06
ORD IDord-15ba9e5435da4645b9b14cb78f297770
Source noteuspto-grants-1989_06