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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1785425Erstellt: 25. Oktober 2026

Potassium Iodide → [2-(3-Cyano-phenyl)-1-methyl-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1785425

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktSodium CyanideHCID 8929—
Edukttert-butyl N-[1-(3-bromophenyl)propan-2-yl]carbamateHCID 69066642—
KatalysatorCopper iodideHCID 83717—
LösungsmittelTolueneHCID 1140—
Produkt[2-(3-Cyano-phenyl)-1-methyl-ethyl]-carbamic acid tert-butyl esterHCID 69068307—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

To a sealed pressure tube was added [2-(3-bromo-phenyl)-1-methyl-ethyl]-carbamic acid tert-butyl ester (1.23 g, 3.9 mmol), sodium cyanide (250 mg, 5.1 mmol), potassium iodide (130 mg, 0.8 mmol), N-N′-dimethylethylenediamine (0.41 mL, 3.9 mmol), and toluene (6 mL). This suspension was then sparged with nitrogen prior to adding copper iodide (150 mg, 0.8 mmol). Reaction mixture heated to 130° C. for 16 h while stirring. Reaction partitioned between ethyl acetate and 30% aqueous ammonia. Organic washed with saturated ammonium chloride, then dried over magnesium sulfate. Reaction reduced to an oil under vacuum and isolated as a white solid after purification on silica. M+1=261.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07504403B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-95b831007d3a45b8a724f5ec6009c0d9
Quellennotizuspto-grants-2009_03