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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640084Generated: October 30, 2026

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

https://huagongshe.com/reaction/640084

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 numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-dab5586ef2904266bc3be96004f61366
Source noteuspto-grants-2010_04