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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709779Generated: October 29, 2026

3-(Benzyloxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-(2-fluoro-5-methoxyphenyl)pyridine → 5-(((Tert-butyldimethylsilyl)oxy)methyl)-2-(2-fluoro-5-methoxyphenyl)pyridin-3-ol

https://huagongshe.com/reaction/709779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Benzyloxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-(2-fluoro-5-methoxyphenyl)pyridineHCID 131733916—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-(((Tert-butyldimethylsilyl)oxy)methyl)-2-(2-fluoro-5-methoxyphenyl)pyridin-3-olHCID 131733917103.5%

Reaction Steps

Under a hydrogen atmosphere, a mixture of 3-(benzyloxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-(2-fluoro-5-methoxyphenyl)pyridine (2.81 g), 10% palladium-activated carbon (280 mg) and ethyl acetate (30 mL) was stirred at room temperature for 30 min. The catalyst was filtered off, and the solvent in the filtrate was evaporated under reduced pressure to give the title compound (2.33 g) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-2ca4c48aca034a86b36c936bb8ad4614
Source noteuspto-grants-2015_11