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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414482Generated: October 26, 2026

Ethanol → ethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylate

https://huagongshe.com/reaction/2414482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
Reactant(2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acidHCID 69270394—
Productethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylateHCID 2214225650%

Reaction Steps

Sulfuric acid (50 ml) was added to (2Z)-2-(2-bromo-4-methoxyphenoxy)-2-butenedioic acid (24.3 g, 86.6 mmol; as prepared in Reference Example 2b above). After heating the mixture with a heat gun for 5-10 min a clear deep brown solution was obtained. This solution was slowly added to refluxing absolute ethanol (250 ml). After the addition the reaction was refluxed for 30 min then allowed to cool. Crystals started to form after 20 min and the reaction was put in the refrigerator overnight. The solid was filtered, washed with cold ethanol/water 9:1 and dried to give ethyl 8-bromo-6-methoxy-4-oxo-4H-chromene-2-carboxylate as an off-white solid (12.3 g, 50% yield, mp 159-161° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06812225B2
Source datasetuspto-grants-2004_11
ORD IDord-38cff3927c3c4a27a801a8c9b004e7b7
Source noteuspto-grants-2004_11