Improving the Performance of Palladium-Catalyzed Telomerization of 1,3-Butadiene with Malonate by Alcohol Solvent
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Chen, Xuan
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East China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
East China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R ChinaEast China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
Chen, Xuan
[1
,2
]
Shen, Chaoren
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East China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
East China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R ChinaEast China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
Shen, Chaoren
[1
,2
]
Don, Kaiwu
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East China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
East China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
East China Normal Univ, Chang Kung Chuang Inst, Sch Chem & Mol Engn, Shanghai 200062, Peoples R ChinaEast China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
Don, Kaiwu
[1
,2
,3
]
机构:
[1] East China Normal Univ, Sch Chem & Mol Engn, State Key Lab Mol & Proc Engn, Shanghai 200062, Peoples R China
[2] East China Normal Univ, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[3] East China Normal Univ, Chang Kung Chuang Inst, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China
Using alcohol instead of largely excessive malonate as thesolvent can improve the performance of palladium-catalyzed telomeri-zation of 1,3-butadiene with malonate. Under the basic conditions, themain reaction was not overwhelmed by the telomerization of 1,3-buta-diene with methanol solvent. With this method, methyl (E)-deca-4,9-di-enoate, the intermediate for the synthesis of 10-hydroxy decanoic acid,undecanedioic acid, and 11-hydroxy undecanoic acid, can be preparedfrom the telomerization of 1,3-butadiene with dimethyl malonate ingood yield.
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Univ Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, SpainUniv Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Balbino, Joao M.
Dupont, Jairton
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Univ Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Univ Nottingham, Sch Chem, Univ Pk, Nottingham NG7 2RD, EnglandUniv Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Dupont, Jairton
Bayon, J. Carles
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Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, SpainUniv Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
机构:
Univ Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, SpainUniv Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Balbino, Joao M.
Dupont, Jairton
论文数: 0引用数: 0
h-index: 0
机构:
Univ Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Univ Nottingham, Sch Chem, Univ Pk, Nottingham NG7 2RD, EnglandUniv Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil
Dupont, Jairton
Bayon, J. Carles
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h-index: 0
机构:
Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, SpainUniv Fed Rio Grande do Sul, Inst Chem, Ave Bento Goncalves 9500, BR-91501970 Porto Alegre, RS, Brazil