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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691162Generated: November 3, 2026

Acetic Acid → 2-(2-Fluoro4-(2-nitro-ethyl)-phenoxymethyl)pyridine

https://huagongshe.com/reaction/1691162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(2-Fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)pyridineHCID 59255141—
SolventWaterHCID 962—
Product2-(2-Fluoro4-(2-nitro-ethyl)-phenoxymethyl)pyridineHCID 5925508049.8%

Reaction Steps

To a dimethyl sulfoxide (30.0 mL) solution of 2-(2-fluoro-4-((E)-2-nitro-vinyl)-phenoxymethyl)-pyridine (3.00 g, 10.9 mmol) described in Manufacturing Example 87-1-2 and acetic acid (3.00 mL) was added sodium borohydride (660 mg, 17.4 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 20 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 crystallized with a tetrahydrofuran-ethyl acetate-heptane system and filtered to obtain the title compound (1.50 g, 49.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-db96752e576f470fb60e15ee1189c8be
Source noteuspto-grants-2012_04