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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263625Generated: November 2, 2026

Hydrochloric Acid → 3,4-Difluorobenzaldehyde

https://huagongshe.com/reaction/263625

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 mole) of ortho-difluorobenzene in 250 ml. of methylene chloride is added to 100 g. (0.75 mole) of anhydrous aluminum chloride. The mixture is stirred (motor) and cooled in an ice bath while 85.5 g. (0.75 mole) 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 unreacted residue of aluminum chloride is washed with methylene chloride until colorless, and the washings are added to the water. The mixture is shaken well in a separation funnel until the methylene chloride layer is green. The organic layer is washed with saturated potassium carbonate solution until neutral, then dried (MgSO4) and distilled to give 3,4-difluorobenzaldehyde, B.P. 70°-74°/20 min. The dark residue in the distillation pot solidifies on cooling to give tris-(3-4,difluorophenyl)methane, M.P. 95°-96°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643959
Source datasetuspto-grants-1997_07
ORD IDord-106f133beccd4a09af66632237cf55f9
Source noteuspto-grants-1997_07