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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 489853Erstellt: 24. Oktober 2026

Acetonitrile → 3-Iodobenzoylacetonitrile

https://huagongshe.com/de/reaction/489853

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
EduktDiisopropylamineHCID 7912—
EduktTetrahydrofuranHCID 8028—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 4-iodobenzoateHCID 142891—
EduktLithium diisopropylamideHCID 2724682—
EduktButyllithiumHCID 178418339—
Produkt3-IodobenzoylacetonitrileHCID 11623179—

Reaktionsbedingungen

Temperatur-50 °C

Reaktionsschritte

n-Butyllithium (30.5 ml, 76 mmol, 2.5 M solution in hexane) was added dropwise to a cooled (0° C.) solution of diisopropylamine (10.6 ml, 76 mmol) in 10 ml dry tetrahydrofuran. Once addition was complete, the solution was kept at 0° C. for 10 minutes and was then cooled to −50° C. This cold LDA solution was then added to a −50° C. solution of acetonitrile (2.37 ml, 45.3 mmol) and ethyl 4-iodobenzoate (10.0 g, 36.2 mmol) in dry tetrahydrofuran (18 ml). Once addition was complete, the reaction was stirred at −50° C. for 3 hours and was subsequently warmed to 0° C. Saturated ammonium chloride was added (20 ml) and the reaction mixture was allowed to warm to room temperature. The product was extracted into ether and washed with 1N hydrochloric acid (50 ml). The organics were washed with brine (50 ml), dried over MgSO4 and then concentrated in vacuo to a red oil. The oil was purified through a small plug of silica gel using 3:1-2:1 hexanes/ethyl acetate as eluent. Concentration of the column fractions in vacuo gave 2-(3-iodobenzoyl)-acetonitrile (8.3 g) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06979693B2
Quelldatensatzuspto-grants-2005_12
ORD IDord-ac2908809536465282098e9b8f1f3314
Quellennotizuspto-grants-2005_12