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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111100Generated: October 30, 2026

Ethyl 2-(4-chlorophenoxy)acetoacetate → Ethyl 5-chloro-3-methylbenzofuran-2-carboxylate

https://huagongshe.com/reaction/1111100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(4-chlorophenoxy)acetoacetateHCID 15678688—
SolventSulfuric AcidHCID 1118—
ProductEthyl 5-chloro-3-methylbenzofuran-2-carboxylateHCID 1564381965%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2 (4-chlorophenoxy)acetoacetate (90.3 g, 0.353 mol) was added dropwise to sulfuric acid (240 ml) stirred at 0° C. The resulting suspension was stirred at 0° C. for 3.5 hours, poured onto crushed ice and the mixture stirred for 0.5 hours. The mixture was extracted with toluene and the organic phase was washed with 5% sodium bicarbonate and water. The organic phase was dried with magnesium sulfate, filtered and concentrated. The crude product was recrystallized from cyclohexane to give 54.5 g (65%) of ethyl 5-chloro-3-methyl-2-benzofuran carboxylate: mp 80°-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04978660
Source datasetuspto-grants-1990_12
ORD IDord-f95b56b889214ce3af0583ae4040572d
Source noteuspto-grants-1990_12