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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576263Generated: October 29, 2026

1-Bromo-2-nitrobenzene → 7-Bromoindole

https://huagongshe.com/reaction/576263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product7-BromoindoleHCID 2757020—

Reaction Conditions

Temperature-40 °C

Reaction Steps

1-bromo-2-nitrobenzene (6.000 g, 29.7 mmol) was added to tetrahydrofuran (65 mL) and cooled to −40° C. Vinylmagnesiumbromide (1M in tetrahydrofuran, 89 mL) was added quickly. The solution was stirred for 20 minutes and then poured into a saturated aqueous solution of ammonium chloride. The solution was extracted with diethyl ether and dried with brine and anhydrous sodium sulfate. The solution was concentrated and purified by flash column chromatography on silica gel with 5% ethyl acetate in hexanes to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035047B2
Source datasetuspto-grants-2015_05
ORD IDord-1f64858cb1304063b65273219b11375e
Source noteuspto-grants-2015_05