HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18502Generated: October 25, 2026
Ammonium Chloride → 7-fluoro-2-methyl-1H-indole
https://huagongshe.com/reaction/18502
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | HCID 178456138 | HCID 178456138 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-fluoro-2-methyl-1H-indole | HCID 15104423 | — |
Reaction Steps
1600 ml of a 0.5M solution of isopropenylmagnesium bromide in THF are cooled to −25° C. under an argon atmosphere, a solution of 37.65 g of 2-fluoronitrobenzene in 250 ml of THF is then added dropwise and the mixture is left stirring at −20° C. for 1 hour. The reaction mixture is poured into a saturated NH4Cl solution, the aqueous phase is extracted with ether and the combined organic phases are concentrated under vacuum. The residue is taken up in water and extracted with DCM, the organic phase is washed with water and with a saturated NaCl solution and dried over MgSO4, and the solvent is evaporated under vacuum. The residue is chromatographed on silica gel, elution being carried out with a cyclohexane/EtOAc mixture (95/5; v/v). 12.35 g of the expected compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741363B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-574c4a03c68d4feba70665e423d45be3 |
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| Source note | uspto-grants-2010_06 |
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