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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716659Generated: October 27, 2026

4-Bromo-2-nitroanisole → 4-Bromo-7-methoxy-1H-indole

https://huagongshe.com/reaction/1716659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-nitroanisoleHCID 118533—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-7-methoxy-1H-indoleHCID 468355408%

Reaction Steps

To a −60° C. solution of 4-bromo-2-nitroanisole (7.89 g, 33.3 mmol) in THF (300 was added vinylmagnesium bromide (1 M in THF, 100 ml, 0.1 mol) while maintaining the reaction temperature below −40° C. The resulting mixture was stirred allowing the temperature to rise to −40° C. in 2 hours. The reaction mixture was then quenched with a saturated solution of NH4Cl (700 ml) and extracted with Et2O (200 ml). The combined organic layers were washed with brine, dried over MgSO4, filtered, concentrated, and purified through flash chromatography affording 4-bromo-7-methoxyindole LII (594 mg, 8% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-43cf058aca7748dfb87cad6dacbcd266
Source noteuspto-grants-2010_09