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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722399Generated: October 31, 2026

1-Bromo-2-nitrobenzene → 7-Bromo-2-methylindole

https://huagongshe.com/reaction/722399

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178456138HCID 178456138—
SolventTetrahydrofuranHCID 8028—
Product7-Bromo-2-methylindoleHCID 4413081—

Reaction Conditions

Temperature-55 °C

Reaction Steps

27.0 g of 2-bromonitrobenzene are placed in 400 ml of THF. The mixture is placed under nitrogen and cooled to −55° C. and then 800 ml of isopropenylmagnesium bromide at 0.5 M in THF are added dropwise. The mixture is left with stirring for 1 hour and then poured into saturated NH4Cl solution. It is extracted with ether, the extract is evaporated and then the residue is taken up in DCM. It is washed with saturated NaCl solution. It is dried and evaporated and then the residue is chromatographed on silica, eluting with an AcOEt/cyclohexane (1/9; v/v) mixture. This gives 10.7 g of the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138424B2
Source datasetuspto-grants-2006_11
ORD IDord-8995fdecd0bb4973b3c445375ef1fde8
Source noteuspto-grants-2006_11