HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432248Generated: October 25, 2026
Water → 1-Benzenesulfonyl-5-methanesulfonylindole-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1432248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 1-Benzenesulfonyl-5-methylthioindole-2-carboxylic acid methyl ester | HCID 86598855 | — |
| Product | 1-Benzenesulfonyl-5-methanesulfonylindole-2-carboxylic acid methyl ester | HCID 68444372 | — |
Reaction Steps
To a mixture of the compound obtained in Example 22 (1) (3.4 g), tetrahydrofuran (90 ml) and water (45 ml), OXONE (registered trademark) (8.7 g) was added at 0° C. and the mixture was stirred for 20 minutes and at 15 to 30° C. for 1 hour. The mixture was diluted with ethyl acetate. The organic layer was washed with water and dried over sodium-sulfate. The solvent was distilled off under reduced pressure to obtain 3.5 g of a white amorphous 1-benzenesulfonyl-5-methanesulfonylindole-2-carboxylic acid methyl ester as a crude product, which was used in the next reaction without; further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612070B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-adb7738109f14c389c2a829559eace03 |
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| Source note | uspto-grants-2009_11 |
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