HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965457Generated: October 26, 2026
Hydrochloric Acid → 2,6-Dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone
https://huagongshe.com/reaction/965457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Octane | HCID 356 | — |
| Reactant | 2,6-Dichlorobenzoyl chloride | HCID 78392 | — |
| Reactant | 3,4,5-Trimethoxytoluene | HCID 80922 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2,6-Dichloro-2',3',4'-trimethoxy-6'-methyl-benzophenone | HCID 22719953 | — |
Reaction Steps
A mixture of 3,4,5-trimethoxytoluene (9.11 g; 50 mmol), octane (25 ml) and iron(III)chloride (50 mg) is stirred at 105° C., and percolating nitrogene 2,6-dichlorobenzoylchloride (12.04 g; 57.5 mmol) is added dropwise within 15 minutes. The mixture is kept at 105° C. and stirred for another 15 minutes. After cooling to 50° C. ethylacetate (50 ml) is added, the mixture shaken twice with 2N hydrochloric acid, once with water and dried. The ethylacetate is evaporated (70° C.) and the liquid cooled with stirring. At 50° C. petrolether (50 ml) is added. The white crystalls formed are sucked off, washed with petrolether and dried. Yield 12.55 g (70.7%), mp. 92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773663 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-551fa88e59804f848f52169121298cf6 |
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| Source note | uspto-grants-1998_06 |
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