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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 5-Chloro-6-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 68726997 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Chloro-6-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 68724257 | 73.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534788B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-989ca13e8f084b37908bda4533a9a35e |
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| Source note | uspto-grants-2009_05 |
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