Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417093Generated: October 29, 2026

(6-Benzyloxy-pyridin-3-yloxy)-acetic acid ethyl ester → (6-Hydroxy-pyridin-3-yloxy)-acetic acid ethyl ester

https://huagongshe.com/reaction/417093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Benzyloxy-pyridin-3-yloxy)-acetic acid ethyl esterHCID 66619330—
CatalystPalladiumHCID 23938—
Product(6-Hydroxy-pyridin-3-yloxy)-acetic acid ethyl esterHCID 17847301491%

Reaction Steps

The suspension of 0.64 g (2.23 mmol) (6-benzyloxy-pyridin-3-yloxy)-acetic acid ethyl ester and 0.064 g 10% palladium on charcoal was hydrogenated for 1 h at 1.7 bar. The reaction mixture was filtered over Dicalite Speed Plus, washed with ethanol and the filtrate was treated with silica gel and evaporated. The residue was purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) with a gradient from heptane:ethyl acetate (100:0 to 0:100) followed by ethyl acetate:methanol (100:0 to 50:50) to give the product as a colorless solid (91%). MS (Turbo Spray): m/z=198.0 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088930B2
Source datasetuspto-grants-2012_01
ORD IDord-5eee0917329147eb875c388903569cef
Source noteuspto-grants-2012_01