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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640359Generated: October 29, 2026

Acetic Acid → 2-(3-Fluoro-4-(2-nitro-ethyl)-phenoxymethyl)-pyridine

https://huagongshe.com/reaction/640359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(3-Fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridineHCID 59255227—
SolventWaterHCID 962—
Product2-(3-Fluoro-4-(2-nitro-ethyl)-phenoxymethyl)-pyridineHCID 5925540550.8%

Reaction Steps

To a dimethyl sulfoxide (20.0 mL) solution of 2-(3-fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridine (1.20 g) described in Manufacturing Example 95-1-2 and acetic acid (1.00 mL) was added sodium borohydride (249 mg, 6.57 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, followed by crystallization with an ethyl acetate-heptane system and filtration to obtain the title compound (614 mg, 50.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691882B2
Source datasetuspto-grants-2010_04
ORD IDord-a6497efaac9048968bfb072ba48dcaa3
Source noteuspto-grants-2010_04