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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17622Erstellt: 23. Oktober 2026

Methyl iodide → tert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamate

https://huagongshe.com/de/reaction/17622

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktTert-butyl (3-tri-n-butylstannylcyclopent-2-enyl)carbamateHCID 15630117—
LösungsmittelDimethylformamideHCID 6228—
Produkttert-Butyl methyl-(3-tri-n-butylstannylcyclopent-2-enyl)carbamateHCID 6858496996,1%

Reaktionsschritte

Tert-butyl (3-tri-n-butylstannylcyclopent-2-enyl)carbamate (2.0 g, 4.24 mmol) was dissolved in N,N-dimethylformamide (40 ml), and at 0° C., methyl iodide (527 μl, 8.47 mmol) and then sodium hydride (55%, w/w), (277 mg, 6.35 mmol) were added. With gradually warming from 0° C. up to room temperature, this was stirred for 24 hours. At 0° C., aqueous saturated ammonium chloride solution was added to the solution, followed by stirring at the same temperature for 30 minutes. The solution was extracted three times with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=99:1, v/v) to obtain a colorless oil (1.982 g, 96%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737166B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-6e43b11caf5d4fa8a96eac542119e500
Quellennotizuspto-grants-2010_06