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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | t-Butyl N-(2-benzoylphenyl)-N-(p-toluenesulfonyl)aminoacetate | HCID 18688807 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | t-Butyl 3-phenyl-1-(p-toluenesulfonyl)indole-2-carboxylate | HCID 18688802 | 115.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE036832 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-a881e6cca260493796f869e621065968 |
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| Source note | uspto-grants-2000_08 |
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