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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026318Generated: October 30, 2026

Sodium Hydroxide → HCID 58047468, compound

https://huagongshe.com/reaction/1026318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67778471HCID 67778471—
SolventMethanolHCID 887—
ProductHCID 58047468HCID 5804746893.6%

Reaction Steps

To a solution of 5-ethoxy-2-[(trimethylsilyl)ethynyl]pyridine (2.74 g) in methanol (40 mL) was added 8M aqueous sodium hydroxide solution (3.73 mL) at room temperature, and the reaction mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate and water, and the aqueous layer was separated from the organic layer. The separated aqueous layer was extracted again with ethyl acetate. The combined organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound as a pale-brown powder (1.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-83a8e0173ba2432fb5fb02f19bfdabd9
Source noteuspto-grants-2014_05