HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432272Generated: October 31, 2026
Hydrochloric Acid → 2-(2-Ethoxycarbonylfuran-5-yl-methyl)-5-methanesulfonylindole
https://huagongshe.com/reaction/1432272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Benzenesulfonyl-2-(2-ethoxycarbonylfuran-5-yl-methyl)-5-methanesulfonylindole | HCID 22504442 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Ethoxycarbonylfuran-5-yl-methyl)-5-methanesulfonylindole | HCID 22504450 | — |
Reaction Steps
To a solution of the compound obtained in Example 30 (4) (0.1722 g) in ethanol (14 ml), potassium hydroxide (0.047 g) was added and the mixture was stirred at 15 to 30° C. for 30 minutes. To the mixture was added 10% aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel column chromatography (hexane:ethyl acetate=0.1:1) to obtain 0.07.48 g of the desired product.
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-645d93fef46149709b17645d0aa43247 |
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| Source note | uspto-grants-2009_11 |
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