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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

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

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846960B2
Source datasetuspto-grants-2010_12
ORD IDord-d272594452704323af16f42de606ddd2
Source noteuspto-grants-2010_12