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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691006Generated: October 25, 2026

Acetic Acid → 4-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridine

https://huagongshe.com/reaction/1691006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridineHCID 59255134—
SolventWaterHCID 962—
Product4-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridineHCID 5925521635.1%

Reaction Steps

To a dimethyl sulfoxide (50 mL) solution of 4-methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine (3.10 g, 11.5 mmol) described in Manufacturing Example 43-1-3 and acetic acid (3.10 mL) was added sodium borohydride (733 mg, 18.4 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 10 minutes. Water was then added dropwise into the reaction solution at room temperature while cooling appropriately, and the reaction mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:5→1:2) to obtain the title compound (1.10 g, 35.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-389950ae8b3e4f6f8858b621c039db6b
Source noteuspto-grants-2012_04