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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9H-carbazole-2-carbaldehyde | HCID 12169810 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-Ethyl-9H-carbazole-2-carbaldehyde | HCID 15134195 | 61.4% |
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
| 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-ddc306f74e5043d5bdfdb78efb8e0900 |
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| Source note | uspto-grants-2011_12 |
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