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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203384Generated: October 31, 2026

Hydroxylamine → 4,4,5,5,5-Pentafluoro-1-(pyridin-2-yl)pentan-1-amine

https://huagongshe.com/reaction/2203384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantSodium HydroxideHCID 14798—
Reactant1-Pentanone,4,4,5,5,5-pentafluoro-1-(2-pyridinyl)-HCID 86679022—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
SolventTrifluoroacetic acidHCID 6422—
Product4,4,5,5,5-Pentafluoro-1-(pyridin-2-yl)pentan-1-amineHCID 88545496—

Reaction Conditions

Temperature25 °C

Reaction Steps

Hydroxylamine (0.216 mL, 3.53 mmol) was added to a solution of 4,4,5,5,5-pentafluoro-1-(pyridin-2-yl)pentan-1-one (0.894 g, 3.53 mmol) in MeOH (10.87 mL) and the resulting solution was stirred at 25° C. for 5 h. Another 1 eq. hydroxylamine was added and the reaction was stirred overnight. Another 2 eq hydroxylamine was added and the reaction was stirred overnight. The reaction mixture was concentrated in vacuo and the resulting residue was diluted with EtOAc and the resulting organic phase was washed with water and brine, then dried (Na2SO4) and concentrated in vacuo to give the crude oxime, as a colorless solid. This was redissolved in TFA (6.52 mL) and cooled to 0° C. Zinc (1.155 g, 17.66 mmol) was added in one portion. After 3 h at 0° C. the reaction mixture was poured into a mixture of ice and 5 N aq. NaOH. The pH was adjusted to pH 10. The mixture was extracted with DCM (3×). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo to give the desired amine product. m/z=255.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365574B2
Source datasetuspto-grants-2016_06
ORD IDord-0a4d34e91aa34624af6457637492f7d2
Source noteuspto-grants-2016_06