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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992350Generated: November 1, 2026

Ethyl Bromide → 4-Ethoxy-1H-indole

https://huagongshe.com/reaction/992350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
Reactant1H-indol-4-olHCID 75421—
SolventDimethylformamideHCID 6228—
Product4-Ethoxy-1H-indoleHCID 15370717—

Reaction Conditions

Temperature0 °C

Reaction Steps

An oven dried two neck flask was charged with 5 ml DMF and NaH (66 mg, 60% in oil, 1.65 mmol). The mixture was cooled down to 0° C., followed by dropwise addition of 4-hydroxy indole (200 mg, 1.5 mmol) in 5 ml DMF over 10 second. After stirring for 30 min under N2, bromoethane in 2 ml DMF was added dropwise, and the reaction was allowed to warm to rt. with continued stirring for 2 hr. Removal of the solvent in vacuo, followed by aqueous work up afforded crude 4-ethoxyindole which was purified by prep. HPLC to afford 201 mg (83%) of pure 4-ethxyindole; HPLC retention time, 1.190 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469006B1
Source datasetuspto-grants-2002_10
ORD IDord-e0fd77c0b1b44a78abab0ce011b61f46
Source noteuspto-grants-2002_10