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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659646Generated: October 29, 2026

Ethyl Bromide → 9-Ethyl-9H-carbazole-2-carbaldehyde

https://huagongshe.com/reaction/659646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant9H-carbazole-2-carbaldehydeHCID 12169810—
SolventDimethylformamideHCID 6228—
Product9-Ethyl-9H-carbazole-2-carbaldehydeHCID 1513419561.4%

Reaction Steps

A 100-mL round-bottom flask was charged with a solution of 9H-carbazole-2-carbaldehyde (3.7 g, 18.97 mmol, 1.00 equiv) in DMF (50 mL). To this was added K2CO3 (5.23 g, 37.90 mmol, 2.00 equiv) followed by addition of bromoethane (10 g, 91.74 mmol, 4.80 equiv). The resulting solution was stirred overnight at room temperature. The reaction progress was monitored by TLC (EA:PE=1:3). Upon completion, the reaction mixture was quenched with water (100 mL). The resulting mixture was extracted with ethyl acetate (3×100 mL), combined organic layers were dried over sodium sulfate and concentrated on a rotary evaporator. The residue was purified by silica gel column chromatography eluted with ethyl acetate/petroleum ether (1:10) affording 9-ethyl-9H-carbazole-2-carbaldehyde as yellow solid (2.6 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080566B1
Source datasetuspto-grants-2011_12
ORD IDord-ddc306f74e5043d5bdfdb78efb8e0900
Source noteuspto-grants-2011_12