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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186039Generated: October 26, 2026

Iodoethane → 3-Ethyl-1,1,2-trimethyl-1H-benzo(e)indol-3-ium Iodide

https://huagongshe.com/reaction/2186039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant2,3,3-TrimethylbenzoindolenineHCID 170530—
SolventAcetonitrileHCID 6342—
Product3-Ethyl-1,1,2-trimethyl-1H-benzo(e)indol-3-ium IodideHCID 1009021591.3%

Reaction Steps

Ethyl iodide (1.1 g, 7.2 mmol) was added to an acetonitrile solution (40 ml) of 1,1,2-trimethylbenz[e]indole (1) (1.0 g, 4.8 mmol, Daiichi Pure Chemicals Co., Ltd.), and then the mixture was heated under reflux for 2 days. The reaction mixture was concentrated under reduced pressure, and ether (80 ml) was added to the residue. The resulting solid was repeatedly washed with ether to obtain the title compound (2) as a dark violet solid (1.6 g, 91%). mp. 213-218° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403625B1
Source datasetuspto-grants-2002_06
ORD IDord-9d9cbc1d84c94af69f860275d98eabac
Source noteuspto-grants-2002_06