Novel Syntheses of Arylcarbamic Esters from Carbon Dioxide and Aromatic Amine via a Zinc Carbamate

Yasuhiko Yoshida, Shigeru Ishii, Akinori Kawato, Tadataka Yamashita, Masahiro Yano, Shohei Inoue

Bulletin of the Chemical Society of Japan · 1988 · 22 citations · 13 references

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Abstract

Abstract Arylcarbamic esters were synthesized directly from carbon dioxide and an aromatic amine via a zinc carbamate. The alkylation of the reaction mixture of carbon dioxide, an aromatic amine, and diethylzinc with dialkyl sulfate formed alkyl arylcarbamate in a high yield. Also, 2-hydroxycyclohexyl diphenylcarbamate was obtained selectively in a good yield by the reaction of carbon dioxide, epoxycyclohexane, and ethylzinc diphenylamide. Other arylcarbamates of 1,2-cyclohexanediol were obtained by the reactions of carbon dioxide, an aromatic amine, diethylzinc, and epoxycyclohexane.

References

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