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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2052903Erstellt: 24. Oktober 2026

Sodium hydride → 7-[2-Oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-heptanoic acid methyl ester

https://huagongshe.com/de/reaction/2052903

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktDimethyl (2-oxoheptyl)phosphonateHCID 580181—
Edukt7-(2-Formyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl esterHCID 85973148—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-[2-Oxo-6-((E)-3-oxo-oct-1-enyl)-piperidin-1-yl]-heptanoic acid methyl esterHCID 10384243106,1%

Reaktionsschritte

Sodium hydride (60% dispersion in oil, 15 mg, 0.37 mmol) was added to a solution of dimethyl 2-oxoheptylphosphonate (87 mg, 0.33 mmol) in THF (2 mL) at 0° C. After 10 min at 0° C., the solution was allowed to warm to rt. After 1 h at rt, the solution was recooled to 0° C. and 7-(2-formyl-6-oxo-piperidin-1-yl)-heptanoic acid methyl ester (crude from previous reaction, ˜0.37 mmol) in THF (2 mL) was added via cannula. The reaction was allowed to warm to rt. After 17 h at rt, the reaction was quenched with acetic acid (50% aqueous, 20 mL) and extracted with EtOAc (3×20 mL). The combined organic phase was washed with saturated aqueous NaHCO3 (20 mL) and brine (20 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient) afforded 128 mg (95%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07326716B2
Quelldatensatzuspto-grants-2008_02
ORD IDord-efd21331e9494d6380134800104f18a4
Quellennotizuspto-grants-2008_02