HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982005Generated: October 29, 2026
5-Bromoindole → 2-(1H-Indol-5-yl)-N,N-dimethylethenesulphonamide
https://huagongshe.com/reaction/982005
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | N,N-dimethylethene-1-sulfonamide | HCID 19037148 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(1H-Indol-5-yl)-N,N-dimethylethenesulphonamide | HCID 54171503 | 38.7% |
Reaction Steps
A mixture of 5-bromoindole (7.7 g), N,N-dimethylethenesulphonamide (5.3 g) triethylamine (15 ml), acetonitrile (5 ml), palladium (II) acetate (0.35 g) and tri-o-tolylphosphine (0.95 g) was heated at 100° C. in an autoclave for 3 h. The resulting cooled mixture was partitioned between hydrochloric acid (2N, 300 ml) and ethyl acetate (2×150 ml). The combined extracts were dried (Na2SO4) and evaporated in vacuo. The residue was purified by `flash` chromatography (V, 7 cm col.) to give the title compound as a crystalline solid (3.8 g) m.p. 148°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04994483 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-d0ff7951d44f4785957f6658ff277433 |
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| Source note | uspto-grants-1991_02 |
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