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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226106Erstellt: 26. Oktober 2026

Methyl iodide → 6-Bromo-2-methylbenzo[B]thiophene

https://huagongshe.com/reaction/226106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktDiisopropylamineHCID 7912—
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukt6-Bromo-benzo[b]thiopheneHCID 12744400—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt6-Bromo-2-methylbenzo[B]thiopheneHCID 2059513195%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Into a stirred solution of diisopropylamine (1.45 mL, 10.3 mmol) and TMEDA (3.4 mL, 22.5 mmol) in THF (30 mL, freshly distilled) at −78° C. is added 1.6 M n-BuLi (7.0 mL, 11.2 mmol) via a syringe. The solution is warmed to 0° C. for 30 min and re-cooled to −78° C. A solution of 6-bromobenzo[b]thiophene 2.0 g, 9.38 mmol) in THF (10 mL) is added via a cannula. After stirring for 30 min, a solution of CH3I (14.0 mL, 28.1 mmol, 2.0 M in tert-butyl methyl ether) is added via a cannula. The solution is stirred overnight, while allowed to warm to room temperature, and diluted with saturated aqueous NaHCO3 (50 mL). The mixture is extracted with Et2O (3×50 mL). The organic layers are combined, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound as a tan solid (2.0177 g, 95%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557103B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-9325051da5144ad2926d2a2174af973f
Quellennotizuspto-grants-2009_07