HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264621Generated: October 28, 2026
Hydrochloric Acid → 7-Chloro-4-methyl-1H-indole
https://huagongshe.com/reaction/2264621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Chloro-3-nitrotoluene | HCID 6976 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Chloro-4-methyl-1H-indole | HCID 26369814 | — |
Reaction Steps
A solution of 5.21 g of 1-chloro-4-methyl-2-nitrobenzene in 150 mL of THF was cooled to −50° C. To the solution was added 95 mL of 1 M vinylmagnesium bromide solution in THF while the inner temperature was kept at −30° C. or lower, and the resulting mixture was stirred at −50° C. for 2 hours. To the solution, 100 mL of the saturated aqueous ammonium chloride solution and 100 mL of 1 M hydrochloric acid were added, then the resulting mixture was warmed to room temperature and stirred for 15 minutes, and then extracted twice with 100 mL of ethyl acetate. The extract was washed with water and saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-hexane=1:9) to obtain 2.69 g of 7-chloro-4-methylindole as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855225B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-4ad822b5c526400b8c9cce6fdaea0d92 |
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| Source note | uspto-grants-2010_12 |
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