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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659615Generated: October 31, 2026

9-Benzyl-3-formylcarbazole → Carbazole-3-carboxaldehyde

https://huagongshe.com/reaction/659615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Benzyl-3-formylcarbazoleHCID 3091534—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductCarbazole-3-carboxaldehydeHCID 50406740%

Reaction Steps

A 250-mL round-bottomed flask was charged with a solution of AlCl3 (9.26 g, 69.45 mmol, 20.00 equiv, 99%) in 1,2-dichloroethane (150 mL). To this was added 9-benzyl-9H-carbazole-3-carbaldehyde (1 g, 3.47 mmol, 1.00 equiv, 99%) in several batches at room temperature over 5 minutes. The resulting mixture was stirred for 2 hours at room temperature. The reaction was then quenched by the addition of H2O/ice (100 mL). The solids were filtered out. The resulting solution was extracted with DCM (3×100 mL) and the combined organic layers were concentrated on a rotary evaporator to give a residue that was purified by silica gel column chromatography eluted with PE:EtOAc (10:1) to afford 9H-carbazole-3-carbaldehyde as green solid (270 mg, 40%). LCMS: [M+H]+: 196

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080566B1
Source datasetuspto-grants-2011_12
ORD IDord-2939eb6eab99484792833ba23d7aeeff
Source noteuspto-grants-2011_12