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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250246Generated: October 26, 2026

Water → 2-(4-Hydroxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/250246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
ReactantBoron tribromideHCID 25134—
Reactant2-(4-Methoxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl esterHCID 57443339—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-(4-Hydroxy-2-methyl-phenyl)-benzo[b]thiophene-5-carboxylic acid ethyl esterHCID 6727159143.4%

Reaction Steps

To a 0° C. 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) is added a 1 M solution of boron tribromide (1.29 mmol; 1.29 mL) in dichloromethane. The reaction 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 over anhydrous sodium sulfate, 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 under reduced pressure and the residue is chromatographed using a gradient of 5% ethyl acetate in hexane to 20% ethyl acetate in hexane to yield the title compound (145 mg, 40%) as a white solid. ES/MS m/e 313 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863302B2
Source datasetuspto-grants-2011_01
ORD IDord-3fa41388b6094c20929339f3a5214a60
Source noteuspto-grants-2011_01