TY - JOUR
T1 - Synthesis of dialkyl hexamethylenedicarbamate from 1,6-hexamethylenediamine and alkyl carbamate over Y(NO3)3·6H2O catalyst
AU - Zhang, Hongzhe
AU - Guo, Xiaoguang
AU - Zhang, Qinghua
AU - Ma, Yubo
AU - Zhou, Hancheng
AU - Li, Jian
AU - Wang, Liguo
AU - Deng, Youquan
PY - 2008/12/10
Y1 - 2008/12/10
N2 - The non-phosgene carbonylation of 1,6-hexamethylenediamine (HDA) with alkyl carbamates using Y(NO3)3·6H2O as a catalyst and the influence of reaction variables on the yields of dialkyl hexamethylenedicarbamate (HDC) were studied. At 453 K and in the presence of 5 wt.% Y(NO3)3·6H2O, nearly 100% HDA conversion and 85% dibutyl hexamethylenedicarbamate (BHDC) isolated yield could be achieved when butyl carbamate (BC) was employed as a carbonyl source. During reaction, an induction period was observed, but it almost disappeared by pretreating the catalyst with n-butanol. The FT-IR, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) characterizations of the catalyst showed that some transformation occurred when the catalyst was pretreated with n-butanol or employed during reaction, i.e., part decomposition of Y(NO3)3 to Y2O3, conversion from crystal to amorphous state, changes occurring in chemical state of the active species, as well as some subtle interactions between the catalyst and n-butanol. All these observed changes might be the reason resulting in activation of the catalyst.
AB - The non-phosgene carbonylation of 1,6-hexamethylenediamine (HDA) with alkyl carbamates using Y(NO3)3·6H2O as a catalyst and the influence of reaction variables on the yields of dialkyl hexamethylenedicarbamate (HDC) were studied. At 453 K and in the presence of 5 wt.% Y(NO3)3·6H2O, nearly 100% HDA conversion and 85% dibutyl hexamethylenedicarbamate (BHDC) isolated yield could be achieved when butyl carbamate (BC) was employed as a carbonyl source. During reaction, an induction period was observed, but it almost disappeared by pretreating the catalyst with n-butanol. The FT-IR, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) characterizations of the catalyst showed that some transformation occurred when the catalyst was pretreated with n-butanol or employed during reaction, i.e., part decomposition of Y(NO3)3 to Y2O3, conversion from crystal to amorphous state, changes occurring in chemical state of the active species, as well as some subtle interactions between the catalyst and n-butanol. All these observed changes might be the reason resulting in activation of the catalyst.
KW - 1,6-Hexamethylenediamine
KW - Alkyl carbamate
KW - Dialkyl hexamethylenedicarbamate
KW - Green chemistry
KW - Non-phosgene
UR - http://www.scopus.com/inward/record.url?scp=55549122625&partnerID=8YFLogxK
U2 - 10.1016/j.molcata.2008.08.020
DO - 10.1016/j.molcata.2008.08.020
M3 - 文章
AN - SCOPUS:55549122625
SN - 1381-1169
VL - 296
SP - 36
EP - 41
JO - Journal of Molecular Catalysis A: Chemical
JF - Journal of Molecular Catalysis A: Chemical
IS - 1-2
ER -