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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantVeratroleHCID 7043—
ReactantTin tetrachlorideHCID 24287—
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
SolventDichloromethaneHCID 6344—
Product(3,4-Dimethoxyphenyl)[4-(trifluoromethyl)phenyl]methanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748634B2
Source datasetuspto-grants-2014_06
ORD IDord-f6eb29e2ecd4411a95ab59c055bd1ba9
Source noteuspto-grants-2014_06