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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493220Generated: November 1, 2026

Hydrochloric Acid → 5-Chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/493220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron tribromideHCID 25134—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant5-Chloro-6-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 68726997—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product5-Chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl esterHCID 6872425773.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

The above prepared 5-chloro-6-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester (2.32 g, 8.63 mmol) was dissolved in 50 mL of CH2Cl2, cooled to 0° C., and treated with BBr3 (17.3 mL of 1M solution in CH2Cl2, 2 eq.). After 5 h at 0° C., the reaction mixture was carefully poured onto crashed ice, twofold extracted with AcOEt, washed with water, dried over magnesium sulfate, and evaporated to dryness. Since substantial amount of free acid had been formed, the crude product was again esterified by treatment with anhydrous HCl in EtOH for 48 h at 48° C. Standard work-up and ensuing flash chromatography (SiO2, hexane/AcOEt=8/2) yielded finally 1.607 g of the title compound as light yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534788B2
Source datasetuspto-grants-2009_05
ORD IDord-989ca13e8f084b37908bda4533a9a35e
Source noteuspto-grants-2009_05