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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 914939Erstellt: 25. Oktober 2026

Dichloromethane → 2-(5-Cyanothien-2-yl)anisole

https://huagongshe.com/reaction/914939

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktSodium CarbonateHCID 10340—
Edukt2-Methoxyphenylboronic acidHCID 2733958—
Edukt5-Bromothiophene-2-carbonitrileHCID 3595059—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-(5-Cyanothien-2-yl)anisoleHCID 2203855196%

Reaktionsschritte

A solution of 5-bromothiophene-2-carbonitrile (1.25 g, 6.65 mmol) in 50 ml of dioxane is degassed with argon, tetrakis(triphenylphosphine)palladium(0) (768 mg, 0.665 mmol) is added and the mixture is stirred for 5 minutes. 2-Methoxybenzene boronic acid (2.02 g, 13.3 mmol) and aqueous 2 N sodium carbonate (13.3 ml) are successively added and the mixture is stirred for 16 hours at 85° C. Extractive work-up (2×50 ml dichloromethane and 2×30 ml water). The organic phase is dried over sodium sulfate, filtrated and evaporated. The residue (4.05 g) is purified via flash chromatography on silica (eluent: 100% hexane>hexane/ethyl acetate 96:4 gradient) to give 1.37 g of 2-(5-cyanothien-2-yl)anisole (96%). M+=215.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07265127B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-7f6f8bdad70240149df90173ba7e59a9
Quellennotizuspto-grants-2007_09