Molecular Formula | C14H14Cl2O2 |
Molar Mass | 285.16 |
Density | 1.366±0.06 g/cm3(Predicted) |
Boling Point | 424.2±40.0 °C(Predicted) |
pKa | 4.25±0.42(Predicted) |
Physical and Chemical Properties | Chemical quality This product is a colorless solid, insoluble in water, soluble in benzene, toluene and other solvents. |
Use | 3-[2-chloro-2-(4-chlorophenyl) vinyl]-2, 2-dimethylcyclopropanecarboxylic acid, abbreviated as chlorpheniramic acid, is an intermediate of fluchlorfenthrin. |
Raw Materials | Gamma Butyrolactone METHYL 3-(2,2-DICHLOROVINYL)-2,2-DIMETHYL-(1-CYCLOPROPANE)CARBOXYLATE 1-Hexene 4-Chlorobenzoyl chloride Methyl 3,3-dimethylpent-4-enoate 4-Chlorostyrene |
Its preparation method is that p-chlorobenzoyl chloride and methyl benzoate react in the presence of SnCl4 to obtain 3, 3-dimethyl-4-p-chlorobenzoyl methyl butyrolactone, and then interact with halogenating agent PCl5 in methanol to generate 3, 3-dimethyl-4, 6-dichloro-6-p-chlorophenylhexene [5] methyl acid, which is dehydrochlorinated under, that is to obtain 3-[2-chloro-2-(4-chlorophenyl) vinyl]-2, 2-dimethylcyclopropanecarboxylic acid methyl ester, further saponification and acidification to obtain the corresponding cyclopropanecarboxylic acid.
chemical properties | this product is a colorless solid, hardly soluble in water, soluble in benzene, toluene and other solvents. |
Use | 3-[2-chloro-2-(4-chlorophenyl) vinyl]-2, 2-dimethylcyclopropanecarboxylic acid is referred to as chlorophenolic acid, which is an intermediate of fluorothrin. |
Production method | The preparation method is that p-chlorobenzoyl chloride and methyl benzoate react in the presence of SnCl4 to obtain 3, 3-dimethyl-4-p-chlorobenzoyl methylbutyrolactone, and then react with the halogenating agent PCl5 in methanol to generate 3, 3-dimethyl-4, 6-dichloro-6-p-chlorophenylhexene [5] acid methyl ester, dehydrochlorinated and cyclized under the action of sodium alkoxide to obtain 3-[2-chloro-2-(4-chlorophenyl) vinyl]-2, 2-dimethylcyclopropanecarboxylic acid methyl ester, further saponification and acidification to obtain the corresponding cyclopropanecarboxylic acid. |