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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant1-Benzenesulfonyl-5-methylthioindole-2-carboxylic acid methyl esterHCID 86598855—
Product1-Benzenesulfonyl-5-methanesulfonylindole-2-carboxylic acid methyl esterHCID 68444372—

Reaction Conditions

Temperature22.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612070B2
Source datasetuspto-grants-2009_11
ORD IDord-adb7738109f14c389c2a829559eace03
Source noteuspto-grants-2009_11