Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095261Generated: October 29, 2026

1-Bromo-2-nitrobenzene → 7-Bromoindole

https://huagongshe.com/reaction/2095261

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 numberUS08445679B2
Source datasetuspto-grants-2013_05
ORD IDord-10d68d11b2004a879c9a21adb4bca6bc
Source noteuspto-grants-2013_05