HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365188Generated: October 26, 2026
4-Bromo-2-nitrotoluene → 4-Bromo-7-methyl-1H-indole
https://huagongshe.com/reaction/2365188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-2-nitrotoluene | HCID 123546 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-7-methyl-1H-indole | HCID 24729279 | 35.3% |
Reaction Steps
To a solution of 4-bromo-2-nitrotoluene (3.0 g, 13.9 mmol) in THF (40 mL) at −40° C. was added vinyl magnesium bromide (48.6 mmol, 48.6 mL; 1.0 M in THF) dropwise over 15 minutes and the mixture stirred at −40° C. for 1.5 hours. The reaction was quenched by the addition of saturated aqueous ammonium chloride and extracted with ethyl acetate. The combined organic layers were washed with brine, separated and dried (MgSO4). The residue was evaporated and purified by column chromatography to yield 4-bromo-7-methylindole (1.03 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08697693B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-40663b4b65fb442b8279d9ff21ef5a6d |
|---|
| Source note | uspto-grants-2014_04 |
|---|