HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261818Generated: October 26, 2026
Water → 2-(4-Hydroxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester
https://huagongshe.com/reaction/2261818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(4-Methoxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester | HCID 57443339 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Hydroxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester | HCID 67271591 | 43.4% |
Reaction Steps
A 0° C. solution of boron tribromide (1M in dichloromethane, 1.29 mmol; 1.29 mL) is added under nitrogen atmosphere to a solution of 2-(4-methoxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester (1.07 mmol; 350 mg) in anhydrous dichloromethane (4.00 mL) and the mixture is stirred at room temperature for 4 h. Water and ethyl acetate are added. The aqueous layer is separated and the organic layer is dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue is dissolved in ethanol (5 mL) and acetyl chloride (3.48 mmol, 0.25 mL) is added. The mixture is stirred at reflux for 5 h. The solvent is removed and the residue is chromatographed (5-20% EtOAc in hexanes) to yield the title compound (145 mg, 40%) as a white solid. LC-ES/MS m/e 313 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846960B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-d272594452704323af16f42de606ddd2 |
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| Source note | uspto-grants-2010_12 |
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