HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165643Generated: October 27, 2026
Benzenesulfonyl chloride → 1H-Indole, 3-acetyl-1-(phenylsulfonyl)-
https://huagongshe.com/reaction/2165643
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 3-Acetylindole | HCID 12802 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1H-Indole, 3-acetyl-1-(phenylsulfonyl)- | HCID 848535 | — |
Reaction Steps
To a solution of 41.39 g of 3-acetyl indole in 300 ml of dimethyl sulfoxide at 0° C. was added a solution of 18.6 g of potassium hydroxide in 20 ml of water. This mixture was stirred at 0° C. for 2 hours, then 47.6 ml of benzenesulfonyl chloride was added dropwise over 40 minutes. The mixture was stirred for an additional 30 minutes, then poured into aqueous ammonium chloride and extracted several times with ether. The ether extracts were combined, washed with water, dried and evaporated, giving 59.8 g of 3-acetyl-N-phenylsulfonyl indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04940710 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-2b93cceae6c045508a234743f73a4884 |
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| Source note | uspto-grants-1990_07 |
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