Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244342Generated: October 26, 2026

N-(4-pentafluoroethyl-benzyl)-2-(3-trifluoromethyl-phenyl)-acetamide → (4-Pentafluoroethyl-benzyl)-[2-(3-trifluoromethyl-phenyl)-ethyl]-amine

https://huagongshe.com/reaction/2244342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-pentafluoroethyl-benzyl)-2-(3-trifluoromethyl-phenyl)-acetamideHCID 86615229—
SolventTetrahydrofuranHCID 8028—
Product(4-Pentafluoroethyl-benzyl)-[2-(3-trifluoromethyl-phenyl)-ethyl]-amineHCID 8661523083.4%

Reaction Steps

Borane-tetrahydrofuran complex solution (1 M in THF, 2.43 mL, 2.43 mmol) was added at 0° C. to a solution of N-(4-pentafluoroethyl-benzyl)-2-(3-trifluoromethyl-phenyl)-acetamide (200 mg, 0.486 mmol) in THF (3.2 mL), and the homogeneous solution was heated at reflux over 90 min. After cooling, excess reagent was destroyed by careful addition of methanol at 0° C. Volatile material was removed by distillation, then the residue was dissolved in 5% ethanolic sulfuric acid solution (2 mL). The solution was refluxed for 2 h, then partitioned between 2 M aq. sodium hydroxide solution and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated. Chromatography (SiO2, heptane-ethyl acetate gradient) afforded the title compound (161 mg, 83%). Colourless oil, MS (ISP) 398.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678818B2
Source datasetuspto-grants-2010_03
ORD IDord-746f2eb7db444a73b31efb24453aaed7
Source noteuspto-grants-2010_03