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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706509Generated: October 29, 2026

1-(3-Methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-one oxime → 1-(3-Methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-amine

https://huagongshe.com/reaction/706509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-one oximeHCID 131733021—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product1-(3-Methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-amineHCID 11811397786.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a stirred solution of 1-(3-methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-one oxime (5.55 g, 18.36 mmol) in acetic acid (40 mL) was added zinc dust (6.00 g, 91.79 mmol). The resulting mixture was heated to 65° C. After 1 h, the mixture was allowed to cool to room temperature and was filtered through Celite. The filtercake was washed with methanol (100 mL). The filtrate was concentrated, and the residue dissolved in 5N ammonium hydroxide solution (75 mL). The mixture was extracted with chloroform (2×50 mL). The combined organic phases were dried over magnesium sulfate, filtered, and concentrated to provide 4.56 g (86%) of 1-(3-methoxy-4-((6-methoxypyridin-3-yl)methoxy)phenyl)ethan-1-amine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174986B2
Source datasetuspto-grants-2015_11
ORD IDord-ff30261f1eb848069ab021b764843250
Source noteuspto-grants-2015_11