![55030-26-7](/CAS/GIF/55030-26-7.gif)
(E)-9-Dodecenoic acid methyl ester synthesis
- Product Name:(E)-9-Dodecenoic acid methyl ester
- CAS Number:55030-26-7
- Molecular formula:C13H24O2
- Molecular Weight:212.33
![Ethylene](/CAS/GIF/74-85-1.gif)
74-85-1
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$79.00/11l
![Methyl dodec-9-enoate](/CAS/20200401/GIF/39202-17-0.gif)
39202-17-0
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![9-Decenoic acid, methyl ester](/CAS2/GIF/25601-41-6.gif)
25601-41-6
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![(E)-9-Dodecenoic acid methyl ester](/CAS/GIF/55030-26-7.gif)
55030-26-7
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![9-Octadecenedioic acid, dimethyl ester](/CAS/20180527/GIF/13481-97-5.gif)
13481-97-5
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Yield:55030-26-7 80 %Chromat.
Reaction Conditions:
with C46H52Br2Cl2N2O3SiW at 20; under 7500.75 Torr; for 2 h;Alkene (Olefin) Metathesis;
Steps:
1.1 Ethenolysis of a mixture of E- and Z-isomers of methyl 9-dodecenoate 1 and 2:
The stock solution of catalyst (prepared according to known methods; TBS = terf.-butyldimethylsilyl) was added to methyl 9-dodecenoate (0.45 ml_, EIZ = 80/20 mixture) and the reaction mixture was pressurized by 10 bar ethylene and stirred at rt for 2 h. Then the pressure was released and MeOH (4.5 ml) was added. An aliquot (200 μΙ_) was taken out and charged onto the top of a silica gel column (0.5 ml silica gel in a 20 ml hypodermic syringe) and the components were eluted with dichloromethane (total DCM used: 25 ml). The eluate was analyzed by gas chromatography. The E-isomer 1 was obtained in a yield of approx. 80 % having a stereoisomeric purity of approx. 96 %. 3 is the ethenolysis product of Z-isomer 2. Compound 4 is formed as a side-product.
References:
WO2018/220088,2018,A1 Location in patent:Paragraph 00119; 00121