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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 642960Erstellt: 25. Oktober 2026

Tetrahydrofuran → Dimethyl-(4-tributylstannylmethoxybutyl)amine

https://huagongshe.com/reaction/642960

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktSodium hydrideHCID 24758—
Edukt4-(Dimethylamino)butan-1-olHCID 83350—
EduktTributyl(iodomethyl)stannaneHCID 10862926—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktDimethyl-(4-tributylstannylmethoxybutyl)amineHCID 5925971671,7%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a mixture of sodium hydride (72%, 232 mg, 7.0 mmol) and tetrahydrofuran (20 ml) was added 4-(dimethylamino)-1-butanol (0.82 g, 7.0 mmol) at 0° C. (external temperature), and the reaction mixture was stirred at 45° C. for 20 minutes. Then, the reaction mixture was cooled at 0° C. (external temperature). To the reaction mixture was added dropwise a mixture of tributyl-iodomethyl-tin (2.0 g, 4.6 mmol) and N,N-dimethylformamide (20 ml) at the same temperature. Then, the reaction mixture was stirred at 45° C. for 30 minutes. The reaction mixture was brought to room temperature, water and ethyl acetate were added to the reaction mixture, and the organic layer was separated. The organic layer was washed with water and an aqueous saturated sodium chloride solution, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethylacetate=20:1, NH silica gel) to obtain the title compound (1.4 g, 3.3 mmol, 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07696347B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-f2badb7377a64c43a05925ac14f44cf8
Quellennotizuspto-grants-2010_04