HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413895Generated: October 27, 2026
Hydrochloric Acid → 2-(9-Ethyl-9H-carbazole-3-carbonyl)benzoic acid
https://huagongshe.com/reaction/1413895
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | N-ethyl carbazole | HCID 6836 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2-(9-Ethyl-9H-carbazole-3-carbonyl)benzoic acid | HCID 20471359 | — |
Reaction Steps
To a mixture of 8.14 g (0.05 mole) of N-ethylcarbazole and 3.7 g (0.025 mole) of phthalic anhydride in 112 g of chlorobenzene, 6.65 g (0.05 mole) of aluminum chloride was added in small increments at ambient temperature after which the mixture was warmed in the range of 50°-70° C. for two hours. The reaction mixture was poured onto ice and rendered acidic by the addition of 10 percent hyrochloric acid. The chlorobenzene layer was separated and steam-distilled to remove the chlorobenzene. The residue was extracted with 10 percent aqueous sodium hydroxide, filtered to remove the insolubles and then acidified with dilute hydrochloric acid. The solid which separated was collected by filtration, washed with water and dried to obtain 2-[(9-ethyl-3-carbazolyl)carbonyl]benzoic acid (Formula VII: R0 =R1 =R2 =Rhu 3=H; R8 =CH2CH3) melting over the range 120°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04251446 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-a3e6171aea3c46bdbeb734256907b96e |
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| Source note | uspto-grants-1981_02 |
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