HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404855Generated: October 30, 2026
Hydrochloric Acid → (3,4-Dimethoxyphenyl)[4-(trifluoromethyl)phenyl]methanone
https://huagongshe.com/reaction/404855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Veratrole | HCID 7043 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 4-(Trifluoromethyl)benzoyl chloride | HCID 67607 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3,4-Dimethoxyphenyl)[4-(trifluoromethyl)phenyl]methanone | HCID 14297391 | — |
Reaction Steps
4-Trifluoromethylbenzoyl chloride (200 grams), 1,2-dimethoxybenzene (128 mL), and dichloromethane (1800 mL) were combined in a reaction flask under a nitrogen atmosphere. Tin (IV) chloride (168 mL) was added to the reaction mixture slowly drop-wise over 45 minutes. The reaction mixture was heated to reflux for 11 hours. It was subsequently cooled to room temperature and slowly poured into a mixture of 200 mL of hydrochloric acid and 1800 mL of ice water. The layers were phase separated. The organic layer was washed with 4 portions of water (1 L each) and then with 1.5 L of 20% saturated aqueous sodium hydroxide (w/v). The organic layer was dried over anhydrous sodium sulfate and then concentrated by rotary evaporation. The residue was recrystallized in 1 L of 15% ethyl acetate/85% hexanes. The crystalline solid was collected by vacuum filtration yielding 132 grams of 3,4-dimethoxy-4′-trifluoromethylbenzophenone. This material was not purified further but was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08748634B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f6eb29e2ecd4411a95ab59c055bd1ba9 |
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| Source note | uspto-grants-2014_06 |
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