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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-nitrotolueneHCID 123546—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-7-methyl-1H-indoleHCID 2472927935.3%

Reaction Conditions

Temperature-40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697693B2
Source datasetuspto-grants-2014_04
ORD IDord-40663b4b65fb442b8279d9ff21ef5a6d
Source noteuspto-grants-2014_04