Synthesis of dialkyl hexamethylene-1,6-dicarbamate from 1,6-hexamethylenediamine and alkyl carbamate over FeCl3 as catalyst

Catalysis Communications

Volumn 10, Issue 8, 2009, Pages 1248-1251

  Guo, Xiaoguang ^a,b   Shang, Jianpeng ^a,b   Ma, Xiangyuan ^a   Li, Jian ^a,b   Zhang, Hongzhe ^a,b   Cui, Xinjiang ^a,b   Shi, Feng ^a   Deng, Youquan ^a  

^a LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

1,6 Hexamethylenediamine; Carbamate; Carbonylation; Isocyanate; Non phosgene

Indexed keywords

CARBONYLATION; CATALYSIS; CYCLOHEXANE; DIRECTIVE ANTENNAS; ESTERIFICATION; ESTERS; LEAD; ZINC;

1,6-HEXAMETHYLENEDIAMINE; BUTYL CARBAMATES; CARBAMATE; ETHYL CARBAMATES; ISOCYANATE; METHYL CARBAMATES; NON-PHOSGENE; OPTIMIZED CONDITIONS; TRANS ESTERIFICATIONS;

CATALYST ACTIVITY;

EID: 61849130093     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2009.01.031     Document Type: Article

References (26)

1. Tundo P., Bressanello S., Loris A., and Sathicq G. Pure Appl. Chem. 77 (2005) 1719-1725
2. Gupte S.P., Shivarkar A.B., and Chaudhari R.V. Chem. Commun. 24 (2001) 2620-2621
3. Curini M., Epifano F., Maltese F., and Rosati O. Tetrahedron Lett. 43 (2002) 4895-4897
4. Tafesh A.M., and Weiguny J. Chem. Rev. 96 (1996) 2035-2052
5. Shi F., and Deng Y. Chem. Commun. 5 (2001) 443-444
6. Li K.T., and Peng Y.J. J. Catal. 143 (1993) 631-634
7. Wehman P., Paul C., Kamer J., and van Leeuwen P.W.N.M. Chem. Commun. 2 (1996) 217-218
8. Alessio E., and Mestroni G. J. Organometall. Chem. 291 (1985) 117-127
9. Ragaini F., and Cenini S. J. Mol. Catal. A 161 (2000) 31-38
10. Kunin A.J., Noirot M.D., and Gladfelter W.L. J. Am. Chem. Soc. 111 (1989) 2739-2741
11. Fu Z.H., and Ono Y. J. Mol. Catal. A 145 (1994) 166-170
12. B. Hans-Josef, K. Heinrich, R. Wolfgang, EP 0 048 371 (1982).
13. Baba T., Fujiwara M., Oosaku A., Kobayashi A., Deleon R.G., and Ono Y. Appl. Catal. A 227 (2002) 1-6
14. Aresta M., Dibenedetto A., Quaranta E., Boscolo M., and Larsson R. J. Mol. Catal. A 174 (2001) 7-13
15. Wang M., Wang H., Zhao N., Wei W., and Sun Y. Catal. Commun. 7 (2006) 6-10
16. H. Peter, K. Klaus, F. Rudolf, F. Kurt, DE 2 943 480 A1 (1981).
17. Li Q., Wang J., Dong W., Kang M., Wang X., and Peng Sh. J. Mol. Catal. A 212 (2004) 99-105
18. G. Laqua, U. Schoner, A. Otterbach, H.V. Schwarz, WO 9 717 323 (1997).
19. F. Merger, F. Towae, US Patent 4 497 963 (1985).
20. Shi F., Deng Y., and SiMa T. Angew. Chem. Int. Ed. 42 (2003) 3257-3260
21. Shi F., Peng J., and Deng Y. J. Catal. 219 (2003) 372-375
22. Baba T., Kobayashi A., Kawanami Y., Inazu K., Ishikawa A., Echizenn T., Murai K., Aso S., and Inomata M. Green Chem. 7 (2005) 159
23. P. Heitkämper, K. Konig, R. Fauss, K. Findeisen, US patent 4 388 238 (1983).
24. Gao J.J., Li H.Q., Zhang Y.F., and Zhang Y. Green Chem. 9 (2007) 572-576
25. F. Merger, F. Towae, US Patent 4 713 476 (1987).
26. Deleon R.G., Kobayashi A., Yamauchi T., Ooishi J., Baba T., Sasaki M., and Hiarata F. Appl. Catal. A 225 (2002) 43-49