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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737069Generated: October 30, 2026

Toluene → 2-Phenyl-4-(2'-trifluoromethyl-biphenyl-4-ylmethyl)-morpholine

https://huagongshe.com/reaction/737069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2-(Trifluoromethyl)benzeneboronic acidHCID 2734387—
Reactant4-(4-Bromo-benzyl)-2-phenyl morpholineHCID 57849504—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product2-Phenyl-4-(2'-trifluoromethyl-biphenyl-4-ylmethyl)-morpholineHCID 1612684969.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

106 mg of 4-(4-Bromo-benzyl)-2-phenyl-morpholine was combined with 91 mg of 2-(Trifluoromethyl)phenyl boronic acid, 18 mg of tetrakis(triphenylphosphine)palladium(0), 1.1 mL of 2M sodium carbonate solution, 2.9 mL toluene and 1.4 mL ethanol. The reaction mixture was heated in a sealed tube at 120° C. overnight in an oil bath. The reaction mixture was filtered through Celite and concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by flash chromatography eluting in a 10 to 40% ethyl acetate/hexanes gradient. The product fractions were pooled and concentrated to afford 88.3 mg of product. ES MS (+) m/z 398

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-e1de05e62a414082b5fe2c464728be32
Source noteuspto-grants-2009_09