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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1613935Erstellt: 26. Oktober 2026

Hexamethylphosphorous triamide → 2-(trans-1-Nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline

https://huagongshe.com/reaction/1613935

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexamethylphosphorous triamideHCID 15355—
EduktOctyltriphenylphosphonium bromideHCID 3084855—
Edukt2-Formyl-3-methyl-4-acetoxy-6-fluoroquinolineHCID 15007058—
EduktButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt2-(trans-1-Nonenyl)-3-methyl-4-acetoxy-6-fluoroquinolineHCID 1500705910,2%

Reaktionsschritte

0.29 ml of a hexane solution of 0.48 mmols of n-butyl lithium was added to a solution of 218 mg (0.48 mmols) of octyltriphenylphosphonium bromide in 3 ml of tetrahydrofuran and stirred at room temperature for 5 minutes. This solution was cooled to -78° C., after which 1.43 g (8 mmols) of hexamethylphosphorus triamide was added and stirred for 5 minutes, followed by further addition of 2 ml of a tetrahydrofuran solution of 98.8 mg (0.40 mmols) of 2-formyl-3-methyl-4-acetoxy-6-fluoroquinoline and stirring at -78° C. for 15 minutes and -42° C. for 30 minutes. The reaction solution was added to 20 ml of water and extracted with ethyl acetate, followed by washing with a saturated sodium chloride aqueous solution and drying with anhydrous sodium sulfate. After removal of the solvent by distillation under reduced pressure, the residue was purified by silica gel column chromatography (solvent n-hexane ethyl acetate=30:1 ) to obtain 14 mg (yield 10 %) of 2-(trans-1-nonenyl)-3-methyl-4-acetoxy-6-fluoroquinoline.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05194617
Quelldatensatzuspto-grants-1993_03
ORD IDord-8c551084591e4f9f836d35e9bd028b88
Quellennotizuspto-grants-1993_03