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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712811Generated: November 1, 2026

Ammonium Acetate → (3-Fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanamine

https://huagongshe.com/reaction/1712811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant(3-Fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanone oximeHCID 72290944—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
SolventAmmonium HydroxideHCID 14923—
Product(3-Fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanamineHCID 5945914893.3%

Reaction Steps

To a suspension of (3-fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanone oxime (904 mg, 3.0 mmol) in EtOH (3 mL) and conc. NH4OH (15 mL) was added ammonium acetate (120 mg, 1.6 mmol) followed by zinc powder (1.05 g, 16.2 mmol) and the reaction mixture was heated at reflux for 2 h. The reaction mixture was allowed to cool to rt then filtered. The filtered solid was washed with 10 N NaOH (15 mL) and EtOAc (15 mL). The combined filtrate was extracted with EtOAc (2×30 mL). The combined organic fractions were washed with sat. NaCl (2×10 mL) then dried over MgSO4, filtered and concentrated under reduced pressure to yield (3-fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanamine (804 mg, 93% yield) as a clear, colorless oil. LCMS: RT=0.96 min [M−NH2] 271.0 (2 min Phenomenex Luna C18 column, 4.6×30 mm eluting with 10-90% acetonitrile/H2O over 2 minutes containing 0.1% TFA; 5 mL/min, monitoring at 220 nm); NMR: 400 MHz 1H (CDCl3) δ ppm 1.68 (bs, 2H), 5.25 (s, 1H), 7.03 (t, J=8.57 Hz, 2H), 7.19 (d, J=7.91 Hz, 1H), 7.29-7.35 (m, 3H), 7.48 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790770B2
Source datasetuspto-grants-2010_09
ORD IDord-2ea595aa05f54577a93eb029780fc5a8
Source noteuspto-grants-2010_09