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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 239233Erstellt: 24. Oktober 2026

Acrylonitrile → Methyl Undecenoate Acrylonitrile

https://huagongshe.com/de/reaction/239233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylonitrileHCID 7855—
EduktMethyl 10-undecenoateHCID 8138—
EduktDodecaneHCID 8182—
EduktSodium benzophenoneHCID 66591377—
EduktMethyl 11-cyano-10-undecenoateHCID 85444428—
Katalysator(1,3-Bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene)(dichloro)((2-((propan-2-yl)oxy)phenyl)methylidene)rutheniumHCID 11763533—
LösungsmittelTolueneHCID 1140—
ProduktMethyl Undecenoate AcrylonitrileHCID 86643178—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

100 mg of methyl 10-undecenoate (0.5 mmol), 53 mg of acrylonitrile (1 mmol) and 10 ml of toluene distilled over sodium-benzophenone are placed in a 50 ml Schlenk tube. 1.5 mg (2.4×10−3 mmol) of second-generation Hoveyda-Grubbs catalyst ((1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(o-iso-propoxyphenylmethylene)ruthenium, available from Aldrich) are added. The mixture is heated to 100° C. and left to react for 1 hour under nitrogen and with magnetic stirring. The reaction mixture is analyzed by gas chromatography (dodecane standard). The conversion of the methyl 10-undecenoate is 94%. The selectivity toward methyl 11-cyano-10-undecenoate (cis+trans mixture) is 100%. The TON (turnover number) is 188.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642792B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-589628850163417e95244eef3e8ebf6c
Quellennotizuspto-grants-2014_02