
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.
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