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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891514Generated: November 3, 2026

Acetic Acid → 2-((4-(2-Nitroethyl)benzyl)oxy)pyridine

https://huagongshe.com/reaction/1891514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-2-((4-(2-Nitrovinyl)benzyl)oxy)pyridineHCID 58076258—
SolventDimethyl SulfoxideHCID 679—
Product2-((4-(2-Nitroethyl)benzyl)oxy)pyridineHCID 5807626677.1%

Reaction Steps

To a solution of 2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine (21.0 g, 81.9 mmol) described in Manufacturing Example 2-1-3, acetic acid (21 mL) in dimethyl sulfoxide (200 mL) was added sodium borohydride (4.96 g, 131 mmol) at room temperature while cooling appropriately. After addition of sodium borohydride, the cooling bath was removed, followed by stirring for 15 minutes at room temperature. The reaction solution was partitioned into water and ethyl acetate. The ethyl acetate layer was washed with water twice and with saturated aqueous sodium chloride once, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:3) to obtain the title compound (16.3 g, 77.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507530B2
Source datasetuspto-grants-2013_08
ORD IDord-10a9f7fb66354055ae3bd93c46680c44
Source noteuspto-grants-2013_08