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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264623Generated: October 31, 2026

Water → HCID 59596797, compound

https://huagongshe.com/reaction/2264623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantIndole-3-Carboxylic AcidHCID 69867—
ReactantPotassium bisulfateHCID 516920—
SolventTetrahydrofuranHCID 8028—
SolventHCID 178418244HCID 178418244—
ProductHCID 59596797HCID 5959679782.5%

Reaction Steps

To a solution of 300 mg of 1H-indole-3-carboxylic acid in 9 mL of THF, 2.68 mL of 1.60 M n-BuLi hexane solution was added dropwise while the inner temperature was kept at −50° C. or lower by cooling in a dry ice-acetone bath, and the resulting mixture was stirred at the same temperature for 5 minutes, then at 0° C. for 1 hour. The solution was cooled in a dry ice-acetone bath and a solution of 461 mg of 4-methoxybenzenesulfonyl chloride in 1 mL of THF was added dropwise. The solution was stirred at 0° C. for 3 hours. To the solution, 20 mL of 5% aqueous potassium hydrogen sulfate solution and 40 mL of water were added in this order, and then the resulting mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. To the residue was added 5 mL of ethyl acetate, and the resulting mixture was stirred at room temperature for 15 minutes. The white crystals formed were collected by filtration to obtain 509 mg of 1-[(4-methoxyphenyl)sulfonyl]-1H-indole-3-carboxylic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855225B2
Source datasetuspto-grants-2010_12
ORD IDord-8d9dedd426964d4c98bcf586d220f09f
Source noteuspto-grants-2010_12