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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 9-Benzyl-3-formylcarbazole | HCID 3091534 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Carbazole-3-carboxaldehyde | HCID 504067 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080566B1 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2939eb6eab99484792833ba23d7aeeff |
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| Source note | uspto-grants-2011_12 |
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