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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78287Erstellt: 24. Oktober 2026

Acetic Acid → 2-Benzyloxy-5-(2-nitro-ethyl)pyridine

https://huagongshe.com/de/reaction/78287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktWaterHCID 962—
EduktVertellusHCID 22959485—
Edukt2-(Benzyloxy)-5-[(E)-2-nitroethenyl]pyridineHCID 56605146—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt2-Benzyloxy-5-(2-nitro-ethyl)pyridineHCID 5925506940,7%

Reaktionsschritte

To a solution of 2-benzyloxy-5-((E)-2-nitro-vinyl)-pyridine described in Manufacturing Example 231-1-3 (44.0 g, 172 mmol) and acetic acid (44.0 mL) in dimethyl sulfoxide (200 mL) was added sodium borohydrate (11.0 g, 275 mmol) at room temperature while cooling appropriately under nitrogen atmosphere, which was stirred for 30 minutes. Water was added to this reaction solution at room temperature while cooling appropriately, which was then partitioned into water and ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (18.1 g, 40.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841327B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-a18c599c3461453e87d6688ff1090134
Quellennotizuspto-grants-2014_09