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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415971Generated: October 25, 2026

5-Amino-2-methylphenol → 4-tert-butyl-N-(3-hydroxy-4-methylphenyl)benzenesulfonamide

https://huagongshe.com/reaction/415971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methylphenolHCID 17818—
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
Reactant4-Tert-Butyl-N-(5-Hydroxy-4-Methyl-2-(2-Oxo-3-Phenylindolin-3-Yl)Phenyl)BenzenesulfonamideHCID 10414540—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product4-tert-butyl-N-(3-hydroxy-4-methylphenyl)benzenesulfonamideHCID 83808378%

Reaction Steps

As another non-limiting example, 4-tert-butyl-N-[5-hydroxy-4-methyl-2-(2-oxo-3-phenyl-2,3-dihydro-1H-indol-3-yl)-phenyl]-benzenesulfonamide (compound 1430) was synthesized by adding dropwise 4-tert-butyl-benzenesulfonyl chloride (8 g, 34 mmol) in 5 mL dichloromethane to a stirring solution of 5-Amino-2-methyl-phenol (4 g, 32 mmol) in 20 mL pyridine and letting the mixture spin overnight at room temperature. The resulting mixture was concentrated in vacuo and the product was purified by column chromatography to yield 8 g (78%) of 4-tert-butyl-N-(3-hydroxy-4-methyl-phenyl)-benzenesulfonamide. A mixture of 3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one (3.9 g, 17 mmol), 4-tert-butyl-N-(3-hydroxy-4-methyl-phenyl)-benzenesulfonamide (7 g, 22 mmol) and p-toluenesulfonic acid (6.5 g, 32 mmol) in dichloroethane was refluxed for 12 hours. The resulting mixture was cooled to room temperature to yield a colorless solid. The solid was filtered and purified using column chromatography to yield 8 g (88%) of the desired product (compound 1430).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088816B2
Source datasetuspto-grants-2012_01
ORD IDord-bacbe40631894ea49c412b1b4f1e1778
Source noteuspto-grants-2012_01