HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527469Generated: November 2, 2026
3-Fluoro-2-trifluoromethyl-pyridine-4-carbaldehyde oxime → 4-Pyridinemethanamine, 3-fluoro-2-(trifluoromethyl)-
https://huagongshe.com/reaction/1527469
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoro-2-trifluoromethyl-pyridine-4-carbaldehyde oxime | HCID 136352325 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Pyridinemethanamine, 3-fluoro-2-(trifluoromethyl)- | HCID 68284147 | — |
Reaction Steps
Zinc dust (0.63 g, 9.62 mmol) was added at RT to a solution of 3-fluoro-2-trifluoromethyl-pyridine-4-carbaldehyde oxime (0.460 g, 1.57 mmol) in acetic acid (8 mL). The reaction mixture was stirred at RT for 3 h, then filtered through a 0.45 microns filter, and the filtrate was concentrated in vacuo. The colored oily residue was partitioned between CH2Cl2 and 1N HCl, the layers were separated and the aqueous phase was extracted twice with CH2Cl2. The pH of the aqueous layer was then adjusted to pH=9 by adding a saturated aqueous NaHCO3 solution, and the resulting white suspension was extracted four times with CH2Cl2. The combined organics were dried (phase separator) and concentrated in vacuo to afford the title compound as a yellow oil. MS (LC/MS): 195.0 [M+H]+; tR (HPLC conditions c): 2.47 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09085555B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-23099a72d800404cb755d54f4a419377 |
|---|
| Source note | uspto-grants-2015_07 |
|---|