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ChemicalBook CAS DataBase List 4-Penten-1-ol
821-09-0

4-Penten-1-ol synthesis

13synthesis methods
-

Yield:821-09-0 97%

Reaction Conditions:

quinoline-2-carboxylic acid;cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate in methanol at 30; for 3 h;Conversion of starting material;

Steps:

1.15

Table 1 shows the results of the deallylation reaction of the ally ethers represented by general formula (I) given above in the case of using a [CpRu(CH3CN)3]PF6-quinaldic acid composite system as the CpRu(II) complex of the present invention. The reaction was carried out in methanol at 30° C. under the condition of [[CpRu(II)(CH3CN)3]PF6]=[quinaldic acid]=1 mM unless otherwise specified.

References:

US2005/203317,2005,A1 Location in patent:Page/Page column 4

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