Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754962Generated: October 28, 2026

Hydrochloric Acid → 5-bromo-6-methyl-1H-indole

https://huagongshe.com/reaction/1754962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ethoxideHCID 2723922—
Reactant(4-Bromo-5-methyl-2-trimethylsilanylethynyl-phenyl)-carbamic acid methyl esterHCID 66816224—
SolventEthanolHCID 702—
SolventSodium chloride; waterHCID 57417360—
Product5-bromo-6-methyl-1H-indoleHCID 2472924166.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

(4-Bromo-5-methyl-2-trimethylsilanylethynyl-phenyl)-carbamic acid methyl ester (506 mg, 1.49 mmol) was dissolved in ethanol (6 ml). Sodium ethoxide (20% solution in ethanol, 1.17 ml, 2.97 mmol) was added and the mixture was stirred at 70° C. overnight. The reaction solution was poured into ice water, and 1 N hydrochloric acid and saturated brine were added to this mixture, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane-ethyl acetate) to give 5-bromo-6-methyl-1H-indole (207 mg, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-ffee61e408fd43899e86637587047854
Source noteuspto-grants-2015_10