HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(1H-indol-5-yl)-N-methylethenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | N-Methylethenesulfonamide | HCID 21895383 | — |
| Catalyst | Tri-o-tolylphosphine | HCID 80271 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(1H-indol-5-yl)-N-methylethenesulfonamide | HCID 13475764 | 28.9% |
Reaction Steps
A mixture of 5-bromoindole (6.6 g), N-methylethenesulphonamide (5.1 g) palladium (II) acetate (75 mg), tri-o-tolylphosphine (0.2 g), triethylamine (12 ml), and acetonitrile (5 ml) was heated at 100° in an autoclave for 3 h. The reaction mixture was cooled and partitioned between hydrochloric acid (1N, 300 ml) and ethyl acetate (2×150 ml). The combined extracts were dried, (Na2SO4) and evaporated in vacuo to give an oil which was purified by `flash` chromatography (Q, 7 cm dia. col.) to give the title compound as a solid (2.3 g) m.p. 164√-166°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994483 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-dbdd133000904a6aa455d06e7c3ac5a1 |
| Source note | uspto-grants-1991_02 |