Technology Process of 1,1-Cyclopropanedicarboxylic acid, 2-ethenyl-, ethyl
4-[(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)oxy]phenyl ester
There total 5 articles about 1,1-Cyclopropanedicarboxylic acid, 2-ethenyl-, ethyl
4-[(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)oxy]phenyl ester which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
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683795-09-7
2-vinyl-cyclopropane-1,1-dicarboxylic acid ethyl ester 4-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyloxy)-phenyl ester
- Guidance literature:
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With
4-pyrrolidin-1-ylpyridine; dicyclohexyl-carbodiimide;
In
dichloromethane;
at 0 - 20 ℃;
for 50h;
DOI:10.1016/j.jfluchem.2003.07.010
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683795-09-7
2-vinyl-cyclopropane-1,1-dicarboxylic acid ethyl ester 4-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyloxy)-phenyl ester
- Guidance literature:
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Multi-step reaction with 2 steps
1: 90 percent / KOH / ethanol / 12 h / 20 °C
2: N,N'-dicyclohexylcarbodiimide; 4-pyrrolidinopyridine / CH2Cl2 / 50 h / 0 - 20 °C
With
potassium hydroxide; 4-pyrrolidin-1-ylpyridine; dicyclohexyl-carbodiimide;
In
ethanol; dichloromethane;
DOI:10.1016/j.jfluchem.2003.07.010
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-
683795-09-7
2-vinyl-cyclopropane-1,1-dicarboxylic acid ethyl ester 4-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-octyloxy)-phenyl ester
- Guidance literature:
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Multi-step reaction with 3 steps
1: 15 percent / PPh3; DEAD / diethyl ether / 97 h / 20 °C
2: 97 percent / aq. KOH / ethanol / 7 h / Heating
3: N,N'-dicyclohexylcarbodiimide; 4-pyrrolidinopyridine / CH2Cl2 / 50 h / 0 - 20 °C
With
potassium hydroxide; 4-pyrrolidin-1-ylpyridine; dicyclohexyl-carbodiimide; triphenylphosphine; diethylazodicarboxylate;
In
diethyl ether; ethanol; dichloromethane;
DOI:10.1016/j.jfluchem.2003.07.010