HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-tetrahydrofuranyl)-5-methanesulfonyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(2-Tetrahydrofuranyl)-5-methanesulfonyl-1-benzenesulfonylindole | HCID 22504449 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2-(2-tetrahydrofuranyl)-5-methanesulfonyl-1H-indole | HCID 22504416 | 82.2% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of the compound obtained in Example 13 (1) (210 mg) in a mixture of tetrahydrofuran/methanol (2:1, 15 ml), a 1N aqueous potassium hydroxide solution (1.6 ml) was added and the mixture was stirred at 100° C. for 2 hours. The reaction solution was then poured into water, extracted with dichloromethane, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was separated using silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) to obtain 113 mg of the desired product as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06875770B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-690d9ee15df94c7b80be0306492847ac |
| Source note | uspto-grants-2005_04 |