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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825631Generated: October 26, 2026

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

https://huagongshe.com/reaction/1825631

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 numberUS07045514B2
Source datasetuspto-grants-2006_05
ORD IDord-41396daf0bc346569e80aa8aef6856bf
Source noteuspto-grants-2006_05