高等学校化学研究 ›› 2010, Vol. 26 ›› Issue (2): 198-203.
MAO Mao1, GU Cheng-zhi2, YIN Hao1, SONG Qin-hua1 and LI Qian-rong1*
MAO Mao1, GU Cheng-zhi2, YIN Hao1, SONG Qin-hua1 and LI Qian-rong1*
摘要:
With the aid of a Pyrolysis-GC/TOF MS technique, the pyrolysis behaviour of two menthyl esters of N-benzoxycarbonyl amino acid was investigated. A clear pattern emerges involving the cleavage of the bond linking the menthyl ring to the carboxy group, followed by further degradation of the fragments. The major pyroproducts were p-menth-1-ene pyrolysed at a higher temperature or p-menth-2-ene pyrolysed at a lower temperature, and various derivatives of cyclohexene pyrolyzed from the menthyl ring. In addition, some of the products were also iden- tified as derivatives of benzene from the pyrolysis of benzyloxyl moiety.