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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47908Generated: October 30, 2026

Sulfuric Acid → HCID 87880875, compound

https://huagongshe.com/reaction/47908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetyl chlorideHCID 6367—
ReactantMagnesiumHCID 5462224—
ReactantHCID 23431777HCID 23431777—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87880875HCID 8788087581.9%

Reaction Conditions

Temperature-30 °C

Reaction Steps

0.1 mol of 3,5-difluoro-2,4,6-trichlorobromobenzene, powder of magnesium (0.11 mol), cuprous chloride (0.12 mol) in 120 ml of THF were stirred at room temperature until the reaction mixture appeared black, which showed the reaction had been initiated. The reaction then was quickly cooled to −30±10° C. GLC was used to monitored the reaction to the completion. Then, to the reaction mixture was added dropwise 11.78 g of acetyl chloride (0.27 mol) in 25 ml of toluene. The reaction was carried out at −30±10° C. for 8 hours. The reaction was then heated to room temperature and stirred for 3 hours. The reactant was poured into 150 g of crushed ice containing 75 ml of 25% sulfuric acid solution and stirred for 5 minutes. The organic layer was separated. The aqueous layer was extracted with toluene. The combined organic layers were washed with aqueous solution (45 ml) of NaCl, aqueous solution (44 ml) of NaHCO3, water (45 ml) and saturated aquoues solution (25 ml) of NaCl, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was recrystallized form ethanol to give 0.0819 mol of 3,5-difluoro-2,4,6-trichloroacteylbenzene in 81.9% yield, mp. 73-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699992B2
Source datasetuspto-grants-2004_03
ORD IDord-db15d1966bee4ae6860a9411d20bc876
Source noteuspto-grants-2004_03