Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Suomen Kemistilehti B called Kinetics of the alkaline and acid hydrolysis of ethyl chloroacetate and β-chloroethyl acetate, Author is Tommila, Eero; Hietala, Sirkku; Nyrkio, Juhani, which mentions a compound: 542-58-5, SMILESS is CC(OCCCl)=O, Molecular C4H7ClO2, Application In Synthesis of 2-Chloroethyl acetate.
In the aqueous alk. hydrolyses, 20 ml. of 0.02M ester and NaOH were mixed; the reaction was stopped by 0.02N HCl, the excess acid titrated with 0.02N Ba(OH)2. K for ClCH2CO2Et (I), and AcOCH2CH2Cl (II) were, resp.: 0.00° 6.59, -; 5.00° -, 0.0733; 10.00° 11.7, -; 15.00° 15.0, 0.155; 25.00° 24.8, 0.330; 40.00° -, 0.932. In the acid hydrolyses, 5 ml. of 0.1M ester and HCl were mixed, and O.02N Ba(OH)2 was used for titration after chilling. K × 105 for I and II at 25.00°, 40.00°, 50.00°, 60.00°; water 8.08, 8.17; 28.9, 33.9; 65.5, 81.8; 138, 193; water + 17.8% acetone 8.49, 7.02; 25.4, 26.7; 58.1, 61.5; 115, 139; water + 27% acetone 8.36, 5.38; 26.5, 20.4; 57.4, 46.3; 112, 104. Activation energies and frequency factors were calculated All corresponding values are given for HCO2Et, AcOEt, and AcOMe.
This literature about this compound(542-58-5)Application In Synthesis of 2-Chloroethyl acetatehas given us a lot of inspiration, and I hope that the research on this compound(2-Chloroethyl acetate) can be further advanced. Maybe we can get more compounds in a similar way.