
Bulletin of the Chemical Society of Japan p. 3486 - 3489 (1990)
Update date:2022-07-30
Topics:
Taguchi, Yoichi
Shibuya, Isao
Yasumoto, Masahiko
Tsuchiya, Tohru
Yonemoto, Katsumi
The trimerization of phenyl isocyanate in the presence of triethylamine was accelerated under high pressure to give triphenyl isocyanurates almost quantitatively.The reaction in benzen was remarkably accelerated by compression.The effects of pressure, temperature, catalysts, and solvents were examined on the trimerization of phenyl isocyanate.Aryl and normal alkyl isocyanates trimerized under high pressure to give the corresponding isocyanurates in good yields, whereas isocynates having bulky alkyl groups such as t-butyl and cyclohexyl did not trimerize even under 800 MPa.
View MoreContact:0086 371 65711996
Address:Jalan 4/3, Kawasan Perindustrian Serendah, 48000 Rawang,
Contact:+86-21-6856-1349 523-87676172
Address:No16 . BinJiang Road . Taixing Economy Developing Area .JiangSu Province . China
Suzhou Kangrun Pharmaceutical, Inc
Contact:86-512-63912376,63913329
Address:Building 2, No. 2358 ,Chang'an Rd, Wujiang Economic Development Zone Pioneering park, china
Beijing Mashi Fine Chemical Co.,Ltd.
Contact:+86-10-61271592
Address:Room 506, Section B, Kaichi Mansion, Industrial Development
Contact:732.938.2777
Address:5012 Industrial Road Farmingdale, NJ 07727
Doi:10.1021/jo972252x
(1998)Doi:10.1016/0040-4039(96)00150-5
(1996)Doi:10.1007/BF02251704
(1999)Doi:10.1016/S0022-328X(97)00635-9
(1998)Doi:10.1039/a800665b
(1998)Doi:10.1016/j.jcat.2003.12.013
(2004)