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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203252Generated: October 31, 2026

2,4,6-Trimethylbenzoyl chloride → HCID 89615123, compound

https://huagongshe.com/reaction/2203252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-Trimethylbenzoyl chlorideHCID 97038—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 89614873HCID 89614873—
SolventDichloromethaneHCID 6344—
ProductHCID 89615123HCID 89615123—

Reaction Steps

To 1-(4-benzo[a]carbazol-11-yl-phenyl)-ethanone (649 mg, 1.93 mmol) in CH2Cl2 (10 mL) are added 2,4,6-trimethylbenzoyl chloride (369 mg, 2.02 mmol) and AlCl3 (1.50 g, 11.24 mmol) at 0° C. After stirring for 0.5 hour, the reaction mixture is stirred for 2 hours at room temperature. The reaction mixture is poured into ice-water, and the crude product is extracted with CH2Cl2. The organic layer is washed with water and brine, dried over MgSO4. After concentration, the crude product is purified by column chromatography on silica gel eluting with a mixed solvent of n-hexane and CH2Cl2 (1:1) to obtain an off-white solid (383 mg; 41%). The structure is confirmed by 1H-NMR spectrum (CDCl3). δ [ppm]: 2.22 (s), 2.41 (s), 2.77 (s), 6.97 (s), 7.15 (d), 7.30-7.34 (m), 7.39 (t), 7.51 (d), 7.63 (d), 7.65 (d), 8.01 (d), 8.28 (d), 8.28 (d), 8.39 (s), 9.53 (d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365515B2
Source datasetuspto-grants-2016_06
ORD IDord-1e0364e24b184fe2aeba611302e70ec4
Source noteuspto-grants-2016_06