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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 590953Erstellt: 23. Oktober 2026

Methyl iodide → 1-Methyl-3-phenylindole

https://huagongshe.com/de/reaction/590953

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
Edukt3-PhenylindoleHCID 96502—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-Methyl-3-phenylindoleHCID 610176100%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Sodium hydride (60% in mineral oil, 200 mg, 5 mmol) was added at 0° C. to a solution of 3-phenyl-1H-indole (1a) (940 mg, 4.86 mmol) in N,N-dimethylformamide (20 mL) under a nitrogen atmosphere. The suspension was stirred for 15 minutes at 0° C. and methyliodide (311 μL, 5 mmol) was then added. The reaction mixture was warmed to room temperature, stirred for 6 hours and then concentrated in vacuo. The residue was partitioned between ethyl acetate (30 mL) and water (10 mL). The organic layer was washed with water (2×10 mL), brine (10 mL), dried over sodium sulfate, filtered and evaporated to dryness to give the desired product (1b) as a yellow oil (1 g, 4.86 mmol, 100%) which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09238026B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-89d5c2fb175646cda65462c0f32c8520
Quellennotizuspto-grants-2016_01