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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510192Generated: October 27, 2026

Ammonium Chloride → 3,4-Difluoro-4'-methoxy-1,1'-biphenyl

https://huagongshe.com/reaction/1510192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-1,2-difluorobenzeneHCID 136519—
Reactant1,3-BIS(2,6-DIISOPROPYLPHENYL)imidazoLIDINIUM-CHLORIDEHCID 18454782—
ReactantHCID 178418443HCID 178418443—
ReactantHCID 178491912HCID 178491912—
SolventTetrahydrofuranHCID 8028—
Product3,4-Difluoro-4'-methoxy-1,1'-biphenylHCID 1531213697%

Reaction Steps

A THF solution of ethylmagnesium bromide (0.55 mL, 1.08 M, 0.60 mmol) was added to CoF2.4H2O (17.0 mg, 0.10 mmol) and 1,3-bis(2,6-diisopropylphenyl)imidazolinium chloride (85.4 mg, 0.20 mmol) at 0° C. under argon atmosphere. The following process was also performed under argon atmosphere. After stirring for four hours at room temperature, 4-chloro-1,2-difluorobenzene (297.0 mg, 2.0 mmol) and a THF solution of p-methoxyphenylmagnesium bromide (3.40 mL, 0.88 M, 3.0 mmol) was added to the mixture. The reaction was performed at 60° C. for 12 hours. After cooled to the ambient temperature, 2.0 mL of saturated ammonium chloride aqueous solution was added to the reaction mixture. The water layer was extracted five times using Et2O. The total organic extract was filtrated by Florisil pad (100-200 mesh, Nacalai Tesque, Inc.). After removing the solvent under reduced pressure, the crude product was purified by silica gel chromatography (toluene=5% in hexane), thereby obtaining the above compound, which was a white solid (0.428 g, yield=97%, purity=>98% (GC analysis)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211820B2
Source datasetuspto-grants-2012_07
ORD IDord-c1846d1a8b1e476884cbadb8e01612fa
Source noteuspto-grants-2012_07