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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350976Generated: October 27, 2026

2-(4-Cyano-3-fluoro-phenoxy)-propionic acid tert-butyl ester → (+)-2-(4-Aminomethyl-3-fluoro-phenoxy)-propionic acid tert-butyl ester

https://huagongshe.com/reaction/350976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Cyano-3-fluoro-phenoxy)-propionic acid tert-butyl esterHCID 23529365—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product(+)-2-(4-Aminomethyl-3-fluoro-phenoxy)-propionic acid tert-butyl esterHCID 2352936495%

Reaction Steps

(±)-2-(4-Cyano-3-fluoro-phenoxy)-propionic acid tert-butyl ester (1.77 g, 6.7 mmol) was shaken on a Parr shaker under 40 psi hydrogen for 30 min, using palladium hydroxide on carbon (1 g, 30% Pd by wt) in 200 mL anhydrous methanol. The reaction mixture was filtered through sintered glass, and solvents removed in vacuo to afford 1.71 g colorless oil (95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183293B2
Source datasetuspto-grants-2007_02
ORD IDord-9febfc997ad1461b942f4072c3052b5a
Source noteuspto-grants-2007_02