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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-2-trifluoromethyl-pyridine-4-carbaldehyde oximeHCID 136352325—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product4-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-23099a72d800404cb755d54f4a419377
Source noteuspto-grants-2015_07