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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656667Generated: November 1, 2026

Chloroethane → N-ethyl carbazole

https://huagongshe.com/reaction/1656667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroethaneHCID 6337—
ReactantCarbazoleHCID 6854—
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantSodium HydroxideHCID 14798—
SolventTriethylamineHCID 8471—
ProductN-ethyl carbazoleHCID 6836—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 0.5-liter autoclave equipped with a stirrer was charged with carbazole (82.0 g), o-dichlorobenzene (100 g), ethyl chloride (40.2 g), 48% sodium hydroxide (73.9 g) and triethylamine (5 g). After the atmosphere in the autoclave was replaced with nitrogen gas, the autoclave was heated to the reaction temperature of 100° C. and the reaction mixture was stirred at the same temperature for 9 hours, while keeping the temperature. After completion of the reaction, the mixture was cooled to 50° C., and was transferred into a separatory funnel. The autoclave was washed with o-dichlorobenzene and water. The washings were combined with the reaction mass, and the combined mixture was separated. The separated organic layer was washed with a 25% sulfuric acid solution to neutralize base traces, and the water layer was removed by separation to give 273.0 g of an o-dichlorobenzene solution of N-ethylcarbazole. The analysis of this solution by chromatography revealed that the content of N-ethylcarbazole was 34.9% and the yield thereof was 99.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254700
Source datasetuspto-grants-1993_10
ORD IDord-c9fa3692eb2e4098846305f7f38fcae5
Source noteuspto-grants-1993_10