126605-22-9Relevant academic research and scientific papers
Catalytic intramolecular participation of amide group in the acid hydrolysis of methyl ether linkage
Arcelli, Antonio,Porzi, Gianni,Sandri, Sergio
, p. 9729 - 9736 (1995)
Evidence for the acid catalyzed hydrolysis or methyl ether linkage assisted by the neighboring amide function was obtained. The hydrolysis rate of 1 to 3 was measured at least 1.7 x 103 fold higher than that of the reference compound 5. The values of thermodynamic parameters suggest that the participation of neighboring amide group in 1 is accompanied by a lower activation enthalphy with respect to the unassisted reaction in 5. Experimental evidence, such as the kinetic isotope ratio, the positive Φ value of Bunnett-Olsen equation and ΔS++ value suggests an A2 mechanism.
Dechlorination of the chloroacetanilide herbicides alachlor and metolachlor by iron metal
Eykholt, Gerald R.,Davenport, Douglas T.
, p. 1482 - 1487 (1998)
Granular iron metal has been found to cause the reductive dechlorination of two important chloroacetanilide herbicides, alachlor and metolachlor. Aqueous solutions (113 mL) of the herbicides were contacted with 40 g of granular cast iron (CCI coarse, 40 mesh) with mild agitation at room temperature. First-order degradation rate constants were 0.12 and 0.10 h-1 for 10 mg/L solutions of alachlor and metolachlor, respectively. A two-site, rate-limited sorption and first-order degradation model was applied to both batch data sets, with excellent agreement for alachlor and fair agreement for metolachlor. The products of the reaction were chloride (84% mass balance for alachlor and 68% for metolachlor) and dechlorinated acetanilides. Supported by GC/EIMS analysis, two sequential reactions may have occurred for alachlor, hydrogenolysis of the chloroacetyl group followed by an N-dealkylation reaction. However, only one product was confirmed by GC/FID, and the mechanism for the N-dealkylation reaction is unknown. Metolachlor was found to produce one dechlorinated product consistent with hydrogenolysis. These results are encouraging, as granular iron may be used at spill sites contaminated with these herbicides and related compounds. Granular iron metal has been found to cause the reductive dechlorination of two important chloroacetanilide herbicides, alachlor and metolachlor. Aqueous solutions (113 mL) of the herbicides were contacted with 40 g of granular cast iron (CCI coarse, 40 mesh) with mild agitation at room temperature. First-order degradation rate constants were 0.12 and 0.10 h-1 for 10 mg/L solutions of alachlor and metolachlor, respectively. A two-site, rate-limited sorption and first-order degradation model was applied to both batch data sets, with excellent agreement for alachlor and fair agreement for metolachlor. The products of the reaction were chloride (84% mass balance for alachlor and 68% for metolachlor) and dechlorinated acetanilides. Supported by GC/EIMS analysis, two sequential reactions may have occurred for alachlor, hydrogenolysis of the chloroacetyl group followed by an N-dealkylation reaction. However, only one product was confirmed by GC/FID, and the mechanism for the N-dealkylation reaction is unknown. Metolachlor was found to produce one dechlorinated product consistent with hydrogenolysis. These results are encouraging, as granular iron may be used at spill sites contaminated with these herbicides and related compounds.
