HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (E)-5-(2-(phenylsulfonyl)vinyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | Phenyl vinyl sulfone | HCID 79664 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-5-(2-(phenylsulfonyl)vinyl)-1H-indole | HCID 15521560 | 85% |
Reaction Steps
A solution of 5-bromoindole (5.0 g, 25.5 mmol), phenylvinylsulfone (7.50 g, 44.64 mmol), Pd(OAc)2 (0.46 g, 2.05 mmol), tri-O-tolylphosphine (1.55 g, 5.10 mmol) and triethylamine (4.88 g, 48.46 mmol) was heated to 95-105° C. for 6-15 h in DMF. The reaction mixture was cooled to RT, diluted with dichloromethane and filtered over a bed of filter aid. The filtrate was sequentially washed with water and brine, and dried over sodium sulphate. The organic layer was concentrated under vacuum and the product precipitated from dichloromethane and hexane as a solid in about 85-90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633239B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-6becbcf7f69841c2875688099706b4fb |
| Source note | uspto-grants-2014_01 |