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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 931694Erstellt: 26. Oktober 2026

Diisopropylamine → Lithium diisopropylamide

https://huagongshe.com/reaction/931694

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktTrimethyltin chlorideHCID 14016—
Edukt4,7-Di(thiophen-2-yl)benzo(c)(1,2,5)thiadiazoleHCID 396294—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktLithium diisopropylamideHCID 2724682—
Produkt2,1,3-Benzothiadiazole, 4,7-bis(5-(trimethylstannyl)-2-thienyl)-HCID 58153009—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Compound (1) was dissolved in anhydrous THF (20 ml) in a nitrogen-filled flask. The solution was cooled down to −78° C. LDA was prepared from the reaction of diisopropylamine (0.5 g, 5.1 mmol, 3 eq.) and n-BuLi (3.12 ml, 5.1 mmol, 3 eq.) (1.6 M hexane solution) in anhydrous THF (2 ml), which was added to the above solution dropwise. After stirring for 1 h, trimethylstannyl chloride (3.8 ml, 3.8 mmol, 2.3 eq.) (1 M THF solution) was added and reacted for 1 h. The reaction was quenched by addition of water and the organic layer was extracted with ether, washed with water and dried over anhydrous magnesium sulfate. After the solvent was removed under reduced pressure, the residue was purified by recrystallization from ethanol, giving the title compound as a needle-shaped purple crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09296864B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-4d36d403e34f4f5eb6ff3d944dfca4b1
Quellennotizuspto-grants-2016_03