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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871818Generated: October 26, 2026

Sodium Methoxide → t-Butyl 3-phenyl-1-(p-toluenesulfonyl)indole-2-carboxylate

https://huagongshe.com/reaction/1871818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactantt-Butyl N-(2-benzoylphenyl)-N-(p-toluenesulfonyl)aminoacetateHCID 18688807—
SolventMethanolHCID 887—
Productt-Butyl 3-phenyl-1-(p-toluenesulfonyl)indole-2-carboxylateHCID 18688802115.3%

Reaction Steps

To a stirred solution of 2.30 g of compound I in 175 cc of methanol was added 0.39 g of sodium methoxide at room temperature and the mixture was stirred for 16 hours. The methanol was distilled off and to the residue was added water, followed by extraction with ethyl acetate. The extract was dried over magnesium sulfate and distilled to remove the solvent. The resulting crude product was dissolved in 50 cc of benzene, followed by adding dropwise thereto 1.41 cc of pyridine and then 0.52 g of thionyl chloride at room temperature, and the resulting mixture was stirred at room temperature for 1 hour. Water was added to the reaction mixture and extracted with ethyl acetate. The extract was dried over magnesium sulfate and distilled to remove the solvent the crude product thus obtained was purified by a silica gel column chromatography (eluent: ethyl acetate/hexane=1/4) to obtain 2.55 g of compound J. Yield: 80.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036832
Source datasetuspto-grants-2000_08
ORD IDord-a881e6cca260493796f869e621065968
Source noteuspto-grants-2000_08