HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611705Generated: October 26, 2026
Hydrochloric Acid → 6,6'-Dimethyl-2,2',3',4'-tetramethoxy-benzophenone
https://huagongshe.com/reaction/611705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3,4,5-Trimethoxytoluene | HCID 80922 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-Methoxy-6-methylbenzoyl chloride | HCID 12892675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6,6'-Dimethyl-2,2',3',4'-tetramethoxy-benzophenone | HCID 15431060 | — |
Reaction Steps
A mixture of 3,4,5-trimethoxytoluene (1.86 g; 10.2 mmol), 1B (10.2 mmol), aluminium chloride (1.33 g, 10 mmol) and dichloromethane (20 ml) is stirred at 0° C. The reaction sets up at 0° C. with formation of hydrogen chloride. Subsequently, the reaction mixture is stirred for another 4 hours at room temperature. A mixture of dilute hydrochloric acid and ethyl acetate (1:1 v/v; 100 ml) is then slowly added at 0° C. The organic phase is concentrated and the residue is recrystallized from methanol. The solid material is collected by vacuum filtration, three times washed with methanol/water (3:1 v/v; 100 ml each) and dried yielding white crystals, 1.0 g (30.3%), mp 84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06001883 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-4ace90345f304c50b8fe97ed6f3d1249 |
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| Source note | uspto-grants-1999_12 |
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