HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172361Generated: November 2, 2026
Dimethylformamide → 11-(Ethylhexyl)-11H-benzo[a]carbazole-5-carbaldehyde
https://huagongshe.com/reaction/2172361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzo[a]carbazole | HCID 9196 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Product | 11-(Ethylhexyl)-11H-benzo[a]carbazole-5-carbaldehyde | HCID 86690527 | 87.7% |
Reaction Steps
To 11H-benzo[a]carbazole (3.00 g, 9.12 mmol) in DMF (7.02 g, 96.1 mmol) is added phosphoryl chloride (14.0 g, 91.3 mmol) at 0° C. After stirring for 2 hours, the mixture is heated at 130° C., and it is stirred for 1 hour. The mixture is cooled at room temperature, and poured into ice-water. The crude product is extracted with CH2Cl2, and it is washed with water and brine. The organic layer is dried over MgSO4. After concentration, the crude product is purified by column chromatography on silica gel eluting with CH2Cl2 to obtain an off-white solid (1.43 g, 43%). The structure is confirmed by 1H-NMR spectrum (CDCl3). δ [ppm]: 0.80-0.90 (m), 1.21-1.46 (m), 2.25 (m), 4.68 (m), 7.40 (t), 7.52-7.60 (m), 7.66-7.74 (m), 8.19 (s), 8.61 (d), 8.64 (s), 9.65 (d), 10.39 (s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051397B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-2c5f8d54ebaf472c8366d7a4ab26c82a |
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| Source note | uspto-grants-2015_06 |
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