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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-nitrobenzene | HCID 11341 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178456138 | HCID 178456138 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Bromo-2-methylindole | HCID 4413081 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138424B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-8995fdecd0bb4973b3c445375ef1fde8 |
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| Source note | uspto-grants-2006_11 |
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