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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352357Generated: November 2, 2026

Ethyl Bromide → HCID 19795531, compound

https://huagongshe.com/reaction/2352357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium HydroxideHCID 14797—
Reactant6-methoxy-3-methyl-1H-indoleHCID 326653—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 19795531HCID 1979553172.2%

Reaction Steps

The 1-ethyl-3-methyl-6-methoxyindol used is prepared as follows: 4.6 g of 3-methyl-6-methoxyindole [Chem. ber. 98, 1727 (1965)] are presented in 29 ml of dimethyl sulfoxide. 6.6 ml of 10n aqueous KOH are then added, and 3.25 g of ethyl bromide are added dropwise at 20° C. in the course of 30'. 1 hour later the reaction mixture is poured onto water and extracted with toluene. Chromatography over silica gel (hexane/ether 5:1) gives 3.9 g of 1-ethyl-3-methyl-6-methoxyindol in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876357
Source datasetuspto-grants-1989_10
ORD IDord-afc28d7626774f6abe0159b14213920a
Source noteuspto-grants-1989_10