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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703229Generated: November 1, 2026

Hydrochloric Acid → 2-(9-Ethyl-9H-carbazole-3-carbonyl)benzoic acid

https://huagongshe.com/reaction/1703229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhthalic AnhydrideHCID 6811—
ReactantN-ethyl carbazoleHCID 6836—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventChlorobenzeneHCID 7964—
Product2-(9-Ethyl-9H-carbazole-3-carbonyl)benzoic acidHCID 20471359—

Reaction Steps

To a mixture of 8.17 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 hydrochloric 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 =R3 =H; R8 =CH2CH3) melting over the range 120°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351768
Source datasetuspto-grants-1982_09
ORD IDord-f676206195f649b092373e8b8c1e66a8
Source noteuspto-grants-1982_09