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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77904Generated: November 3, 2026

Acetic Acid → 5-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridine

https://huagongshe.com/reaction/77904

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridineHCID 59255428—
SolventWaterHCID 962—
Product5-Methyl-2-(4-(2-nitro-ethyl)-benzyloxy)pyridineHCID 5925510354.4%

Reaction Steps

To a dimethyl sulfoxide (40.0 mL) solution of 5-methyl-2-(4-((E)-2-nitro-vinyl)-benzyloxy)-pyridine (3.50 g, 12.9 mmol) described in Manufacturing Example 44-1-3 and acetic acid (3.50 mL) was added sodium borohydride (822 mg, 20.6 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 10 minutes. Water was then added dropwise at room temperature while cooling appropriately. The reaction mixture was extracted with ethyl acetate, and the organic layer was 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=1:4) to obtain the title compound (1.91 g, 54.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-223d43412dc84836ac4a87fd05418469
Source noteuspto-grants-2014_09