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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268785Generated: October 31, 2026

2-Bromo-4-nitroanisole → 4-bromo-5-methoxy-1H-indole

https://huagongshe.com/reaction/268785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitroanisoleHCID 78870—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product4-bromo-5-methoxy-1H-indoleHCID 220305583%

Reaction Steps

To a −40° C. solution of 2-bromo-4-nitro-anisole (1.16 g, 5 mmol) in THF (10 ml) was added vinylmagnesium bromide (1M in THF, 15 ml). The reaction mixture was stirred for 30 min while allowing the temperature to rise to −20° C. The reaction was quenched by addition of a saturated solution of NH4Cl, diluted with Et2O, and the aqueous layer was extracted twice with Et2O. The combined organic layers were dried over Na2SO4, filtered, concentrated, and purified via flash chromatography (hexane/EtOAc) to provide 4-bromo-5-methoxyindole XLVI (38 mg, 3% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446118B2
Source datasetuspto-grants-2008_11
ORD IDord-f21fbc06921944cb872012656c186511
Source noteuspto-grants-2008_11