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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Chloro-3-nitrotolueneHCID 6976—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418507HCID 178418507—
SolventTetrahydrofuranHCID 8028—
Product7-Chloro-4-methyl-1H-indoleHCID 26369814—

Reaction Conditions

Temperature-50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855225B2
Source datasetuspto-grants-2010_12
ORD IDord-4ad822b5c526400b8c9cce6fdaea0d92
Source noteuspto-grants-2010_12