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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52620Generated: October 25, 2026

Water → 2-Amino-6-methyl-5-[3,5-di(trifluoromethyl)phenyl]benzonitrile

https://huagongshe.com/reaction/52620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Bis-trifluoromethylphenylboronic acidHCID 156265—
Reactant6-Amino-3-bromo-2-methylbenzonitrileHCID 22465737—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-Amino-6-methyl-5-[3,5-di(trifluoromethyl)phenyl]benzonitrileHCID 1540528136.3%

Reaction Steps

A stirred solution of 1.7 grams (0.008 mole) of 2-amino-5-bromo-6-methylbenzonitrile, 3.2 grams (0.012 mole) of 3,5-di(trifluoromethyl)phenylboronic acid, 4.3 grams (0.031 mole) of potassium carbonate and 0.3 mL of tetrakis(triphenylphosphine)palladium(0) in 150 mL of toluene was heated at 90° C. for about 20 hours. After this time, the reaction mixture was stirred with 100 mL of water, and the organic layer was separated. The organic layer was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography on silica gel, using 30/65/5 and 20/60/20 methylene chloride/petroleum ether/ethyl acetate as eluants. The product-containing fractions were combined and concentrated under reduced pressure, yielding about 1.0 gram of 2-amino-6-methyl-5-[3,5-di(trifluoromethyl)phenyl]benzonitrile. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616718
Source datasetuspto-grants-1997_04
ORD IDord-9916fa2187804a368c3277d3be25570e
Source noteuspto-grants-1997_04