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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20907Erstellt: 24. Oktober 2026

Toluene → HCID 178514666, Verbindung

https://huagongshe.com/de/reaction/20907

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktEthyl AcetateHCID 8857—
Edukt2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
Edukt2-(6-{2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-pyrrolidin-1-yl}-6-oxo-hexyl)-isoindole-1,3-dioneHCID 131728216—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
ProduktHCID 178514666HCID 17851466689%

Reaktionsschritte

Compound 44a (9.0 g, 13.57 mmol) was coevaporated with anhydrous toluene (50 mL). To the residue N,N-tetraisopropylammonium tetrazolide (0.766 g, 6.8 mmol) was added and the mixture was dried over P2O5 in a vacuum oven for overnight at 40° C. The reaction mixture was dissolved in dichloromethane (20 mL) and 2-cyanoethyl-N,N,N′,N′-tetraisopropylphosphorodiamidite (6.13 g, 6.7 mL, 20.35 mmol) was added. The reaction mixture was stirred at ambient temperature for overnight. The completion of the reaction was ascertained by TLC (Rf=0.7 in 1:1 ethyl acetate:hexane). The reaction mixture was diluted with dichloromethane (100 mL) and washed with 5% NaHCO3 (100 mL) and brine (100 mL). The organic layer was dried over anhydrous Na2SO4 filtered and concentrated under reduced pressure. The residue was purified over silica gel (50:49:1, EtOAc:Hexane:triethlyamine) to afford compound 45a as white solid (10.5 g, 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745608B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-d07b1095f64c4a1f966ce0e280cb68d1
Quellennotizuspto-grants-2010_06