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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693968Generated: November 2, 2026

Acetic Acid → 3-(4-(2-Nitro-ethyl)-phenoxy)-pyridine

https://huagongshe.com/reaction/1693968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59255233HCID 59255233—
SolventWaterHCID 962—
Product3-(4-(2-Nitro-ethyl)-phenoxy)-pyridineHCID 5925527640.6%

Reaction Steps

To a dimethyl sulfoxide (15.0 mL) solution of 3-(4-((E)-2-nitro-vinyl)-phenoxy)pyridine (2.00 g, 8.26 mmol) described in Manufacturing Example 76-1-2 and acetic acid (2.00 mL) was added sodium borohydride (500 mg, 13.2 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes at room temperature. 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=1:3→1:2) to obtain the title compound (819 mg, 40.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-5ebc175ec31e4291b9a19e9380c41744
Source noteuspto-grants-2012_04