Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387942Generated: November 1, 2026

Ethyl Acetate → Tert-butyl 6-bromo-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/1387942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyl acrylateHCID 15458—
Reactant5-BromosalicylaldehydeHCID 72863—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
ProductTert-butyl 6-bromo-2H-chromene-3-carboxylateHCID 10566979—

Reaction Steps

To a solution of 5-bromosalicylaldehyde (10.0 g) and tert-butyl acrylate (17.5 ml) in tert-butanol (100 ml) was added potassium tert-butoxide (1.67 g) at room temperature, and the mixture was refluxed for 66 hours and cooled to room temperature. To the mixture was added ethyl acetate, and the mixture was washed with water, 1N sodium hydroxide and saturated sodium chloride solution, dried with magnesium sulfate and concentrated. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:19) to give tert-butyl 6-bromo-2H-1-benzopyran-3-carboxylate (10.86 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-ea4d59d3720b49f594bf5a198302f6c6
Source noteuspto-grants-2001_07