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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349348Erstellt: 24. Oktober 2026

Sodium hydride → HCID 69020248, Verbindung

https://huagongshe.com/de/reaction/349348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktDimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonateHCID 12989750—
Edukt[4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl esterHCID 86595299—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 69020248HCID 6902024834%

Reaktionsschritte

Sodium hydride (60% dispersion in oil, 35 mg, 0.88 mmol) was added to a solution of [3-(3-chlorophenyl)-2-oxopropyl]-phosphonic acid dimethyl ester (221 mg, 0.80 mmol) in THF (2.0 mL) at 0° C. After 1 h at 0° C., [4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl ester (0.88 mmol, crude) in THF (2 mL) was added via cannula. The reaction was allowed to warm to rt. After 18 h at rt, the reaction was quenched with aqueous acetic acid (50%, 10 mL) and extracted with EtOAc (3×20 mL). The combined organic phase was washed with brine (25 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (20% →40% EtOAc/CH2Cl2, gradient) afforded 117 mg (34%) of (4-{(R)-2-[(E)-4-(3-chlorophenyl)-3-oxo-but-1-enyl]-6-oxo-piperidin-1-yl}-butoxy)-acetic acid ethyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179820B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-0d6484f6104048d9a4bc30d491aac73c
Quellennotizuspto-grants-2007_02