HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 5-bromo-1-(4-methylbenzenesulfonyl)-1H-indole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 5-Bromoindole-3-carbaldehyde | HCID 70137 | — |
| Reactant | Lithium diisopropylamide mono(tetrahydrofuran) | HCID 10997623 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-bromo-1-(4-methylbenzenesulfonyl)-1H-indole-3-carbaldehyde | HCID 10384969 | 248.8% |
Reaction Steps
To a solution of 5-bromoindole-3-carboxaldehyde (10 g) in dry tetrahydrofuran (75 ml), cooled to -78° C., was added with 2M lithium diisopropylamide/tetrahydrofuran (22.5 ml). After 30 min., the mixture was treated with a solution of tosyl chloride (9.5 g) in dry tetrahydrofuran (75 ml). The mixture was allowed to warm to room temperature overnight and evaporated. The residue was dissolved in dimethylformamide, filtered, and the filtrate was diluted with water. The precipitate was collected and recrystallized from ethanol to give 42 g (25%) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597838 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-e741bf75d9bf46b8b8083db07c21467e |
| Source note | uspto-grants-1997_01 |