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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71191Generated: October 28, 2026

2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl → 2-Fluoro-5-methoxy-4-(2-methyl-1,3-oxazol-5-yl)benzonitrile

https://huagongshe.com/reaction/71191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant5-(4-Chloro-5-fluoro-2-methoxyphenyl)-2-methyl-1,3-oxazoleHCID 66608708—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Fluoro-5-methoxy-4-(2-methyl-1,3-oxazol-5-yl)benzonitrileHCID 66607445839.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a mixture of 5-(4-chloro-5-fluoro-2-methoxyphenyl)-2-methyl-1,3-oxazole (1.12 g) and zinc(II) cyanide (0.327 g) in DMF (10 mL) were added tris(dibenzylideneacetone)dipalladium(0) (212 mg) and 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (182 mg) at room temperature, and the mixture was stirred overnight under a nitrogen atmosphere at 130° C. The reaction mixture was diluted with water, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (902 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822699B2
Source datasetuspto-grants-2014_09
ORD IDord-abde0950e4da4af39860badb28f3502b
Source noteuspto-grants-2014_09