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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186576Generated: October 30, 2026

Hydrochloric Acid → 3,4-Difluorobenzaldehyde

https://huagongshe.com/reaction/2186576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2-DifluorobenzeneHCID 9706—
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product3,4-DifluorobenzaldehydeHCID 588088—

Reaction Steps

57 g (0.5 mol) of ortho-difluorobenzene in 250 ml of methylene chloride is added to 100 g (0.75 mol) of anhydrous aluminum chloride. The mixture is stirred mechanically at 0° C. (ice bath) while 85.5 g (0.75 mol) of dichloromethyl methylether is added dropwise. Vigorous HCl evolution takes place, and the reaction mixture turns orange-red. After the addition, the mixture is stirred at room temperature for 15 minutes, and the liquid phase is decanted into 500 ml of ice and water. The residue in the reaction flask is washed with methylene chloride until colorless, and the washings are added to the water. The mixture is shaken well in a separatory funnel until the methylene chloride layer is green. The organic layer is washed with saturated potassium carbonate solution until neutral, is dried MgSO4) and is distilled to give 3,4-difluorobenzaldehyde, B.P. 70-74° C/20 mm. The dark residue in the distillation pot solidifies on cooling to give tris-(3,4-difluorophenyl)methane, M.P. 95-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06403831B1
Source datasetuspto-grants-2002_06
ORD IDord-e9d89b87fb0246e98ca0c6bff9c78ddb
Source noteuspto-grants-2002_06