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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 473006Erstellt: 26. Oktober 2026

Lithium diisopropylamide → 1-(Pyridazin-3-yl)ethan-1-ol

https://huagongshe.com/reaction/473006

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium diisopropylamideHCID 2724682—
Edukt6'-Bromospiro[cyclohexane-1,2'-indene]-1',4(3'H)-dioneHCID 58197205—
EduktN-methoxy-N-methylpyridazine-3-carboxamideHCID 58197546—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Pyridazin-3-yl)ethan-1-olHCID 15197511106,6%

Reaktionsbedingungen

Temperatur-60 °C

Reaktionsschritte

To a solution of LDA (23.4 mL, 42.1 mmol, 1.8 M in THF) in THF (150 mL) was added slowly a solution of compound 1 (3.6 g, 21.05 mmol) in THF (77 mL) at −60° C. under a N2 atmosphere. After being stirred at −60° C. for 1 h, a solution of compound 2 (7.05 g, 18.9 mmol)) in THF (23 mL) was added slowly to the above solution. The resulting mixture was stirred at −60° C. for 2 h. The reaction mixture was quenched with water (15 mL). The aqueous layer was extracted with EtOAc (3×40 mL). The combined organic layers were washed with brine (20 mL), dried over Na2SO4 and concentrated under reduced pressure to dryness. The residue was purified by column chromatography on silica gel (petroleum: ethyl acetate, 10:1) to give compound 3 (2.5 g, yield 26%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633212B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-96c188ef74f441d98b00b71844dc2ec1
Quellennotizuspto-grants-2014_01