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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199734Generated: October 29, 2026

1-Bromo-2-nitrobenzene → 7-Bromoindole

https://huagongshe.com/reaction/2199734

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 numberUS09359296B2
Source datasetuspto-grants-2016_06
ORD IDord-0d3ea9c378374513a072d8c7506debd8
Source noteuspto-grants-2016_06