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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172370Generated: November 1, 2026

2-Methylbenzoyl chloride → HCID 66980798, compound

https://huagongshe.com/reaction/2172370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzoyl chlorideHCID 70276—
Reactant2,4,6-Trimethylbenzoyl chlorideHCID 97038—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 66980816HCID 66980816—
SolventDichloromethaneHCID 6344—
ProductHCID 66980798HCID 6698079821.1%

Reaction Steps

To 7-(2-ethylhexyl)-7H-benzo[c]carbazole (0.66 g, 2.00 mmol) in CH2Cl2 are added AlCl3 (0.27 g, 2.06 mmol) and 2,4,6-trimethylbenzoyl chloride (0.37 g, 2.00 mmol) at 0° C., and then the mixture is stirred for 2 hours. To the reaction mixture are added AlCl3 (0.29 g, 2.20 mmol) and o-toluoyl chloride (0.32 g, 2.06 mmol) at 0° C., and then the mixture is stirred overnight. The reaction mixture is poured into ice-water, and the crude product is extracted with CH2Cl2, and washed with water and brine. After drying over MgSO4 and concentration, the crude product is purified by column chromatography on silica gel eluting with a mixed solvent of CH2Cl2 and n-hexane (4:1) to obtain a white solid (0.25 g, 21%). The structure is confirmed by 1H-NMR spectrum (CDCl3) δ [ppm]: 0.84 (t), 0.93 (t), 1.22-1.45 (m), 2.04-2.09 (m), 2.18 (s), 2.38 (s), 2.39 (s), 4.32-4.34 (m), 6.97 (s), 7.30-7.37 (m), 7.42-7.47 (m), 7.51 (d), 7.68 (d), 7.88 (br), 7.96 (d), 8.21 (dd), 8.37 (d), 8.78 (br), 9.19 (br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051397B2
Source datasetuspto-grants-2015_06
ORD IDord-83ad1cd504ae424b932ba407b5ef036c
Source noteuspto-grants-2015_06