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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046742Generated: November 1, 2026

Benzoyl chloride → HCID 67235106, compound

https://huagongshe.com/reaction/1046742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant9-(2-Ethylhexyl)-9H-carbazoleHCID 16217868—
SolventDichloromethaneHCID 6344—
ProductHCID 67235106HCID 6723510615.6%

Reaction Steps

To a solution of 9-(2-ethyl-hexyl)-9H-carbazole (7.0 g, 0.025 mol) in dichloromethane (30 ml), benzoyl chloride (4.5 g, 0.0525 mol) was added and stirred for 15 minutes at room temperature. Aluminium chloride (7.3 g, 0.055 mol) was added in portions while the temperature was maintained below 30° C. The reaction mixture was allowed to stir at room temperature for 15 hours. The reaction mixture was poured into ice (150 g) and distilled water (100 ml) and diluted with dichloromethane (200 ml). The organic layer was separated and washed with a saturated solution of sodium bicarbonate (250 ml) and a saturated solution of sodium chloride (250 ml). The organic layer was dried over MgSO4, filtered and the solvent was removed under reduced pressure. The residual solid was purified on a Prochrom LC80 Column using ethyl acetate/n-hexane (20/80) as eluent. TLC shows a yellow fluorescent product with Rf-value of 0.48 in dichloromethane as eluent. Evaporation of the pooled fractions yielded 1.5 g of [9-(2-Ethyl-hexyl)-9H-carbazol-3-yl]-phenyl-methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569393B2
Source datasetuspto-grants-2013_10
ORD IDord-4c86fdb04b22410db13f459e8fb1b52f
Source noteuspto-grants-2013_10