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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | (3-Fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanone oxime | HCID 72290944 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | (3-Fluoro-5-(trifluoromethyl)phenyl)(4-fluorophenyl)methanamine | HCID 59459148 | 93.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790770B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-2ea595aa05f54577a93eb029780fc5a8 |
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| Source note | uspto-grants-2010_09 |
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