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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trimethylbenzoyl chloride | HCID 97038 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 89614873 | HCID 89614873 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 89615123 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365515B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-1e0364e24b184fe2aeba611302e70ec4 |
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| Source note | uspto-grants-2016_06 |
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