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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239233Generated: October 25, 2026

Acrylonitrile → Methyl Undecenoate Acrylonitrile

https://huagongshe.com/reaction/239233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantMethyl 10-undecenoateHCID 8138—
ReactantDodecaneHCID 8182—
ReactantSodium benzophenoneHCID 66591377—
ReactantMethyl 11-cyano-10-undecenoateHCID 85444428—
Catalyst(1,3-Bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene)(dichloro)((2-((propan-2-yl)oxy)phenyl)methylidene)rutheniumHCID 11763533—
SolventTolueneHCID 1140—
ProductMethyl Undecenoate AcrylonitrileHCID 86643178—

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642792B2
Source datasetuspto-grants-2014_02
ORD IDord-589628850163417e95244eef3e8ebf6c
Source noteuspto-grants-2014_02