Novel Synthesis of Carbamate Ester from Carbon Dioxide, Amines, and Alkyl Halides
- 1 May 1989
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 62 (5) , 1534-1538
- https://doi.org/10.1246/bcsj.62.1534
Abstract
A novel synthesis of carbamate ester using carbon dioxide as a direct material is reported in this article. The direct reaction of carbon dioxide, aliphatic amines, and alkyl halides was found to give the corresponding alkyl carbamate esters in good yields. Reactions using secondary alkyl bromides gave carbamate esters in higher yields than those using primary or tertiary alkyl bromides. The carbamate ester yields increased with the addition of N,N-dimethylformamide to the reaction system of carbon dioxide, amines and, alkyl halides. This reaction is considered to proceed by an SN2 displacement reaction of the alkyl halide by the carbamate anion formed from the reaction of carbon dioxide and the amine.This publication has 5 references indexed in Scilit:
- Ruthenium-catalyzed synthesis of vinyl carbamates from carbon dioxide, acetylene, and secondary aminesThe Journal of Organic Chemistry, 1987
- Formation of Bis(2-oxazolidinone) Derivatives by Reactions of 2-Methoxy-3,3-dimethyl-2-phenyloxirane or α-Bromoisobutyrophenone with Carbon Dioxide and Aliphatic α,ω-DiaminesBulletin of the Chemical Society of Japan, 1986
- Elimination-addition mechanisms of acyl group transfer: the hydrolysis and synthesis of carbamatesJournal of the American Chemical Society, 1977
- Esters of Carbamic AcidChemical Reviews, 1965
- Über substituierte Hydrazo‐dicarbonamide, Hydrazodithio‐carbonamide und deren UmwandlungsprodukteEuropean Journal of Organic Chemistry, 1954