HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-1-fluoro-2-nitrobenzene → 4-Bromo-7-fluoroindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-1-fluoro-2-nitrobenzene | HCID 2736328 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-7-fluoroindole | HCID 3822541 | 23.4% |
Reaction Steps
At −40° C., vinylmagnesium bromide (300 mL of 1.0M solution in THF, 300 mmol) was added dropwise to a solution of 3-nitro-4-fluoro-bromobenzene (22 g, 100 mmol) in THF (700 mL). After 1 h at −40° C., the mixture was quenched by aqueous NH4Cl solution and extracted by EtOAc. The organic layer was dried over Na2SO4 and concentrated to give the crude product which was purified by silica gel column chromatography affording 4-bromo-7-fluoro-1H-indole (5 g, 23.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133180B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-67a5de6ccea04a9ea54cc5fd323bfe21 |
| Source note | uspto-grants-2015_09 |