73330-91-3Relevant articles and documents
Methoxycarbonylation of Alkyl-, Cycloalkyl-, and Arylamines with Dimethyl Carbonate in the Presence of Binder-Free Zeolite
Khazipova, A. N.,Khusnutdinov, R. I.,Mayakova, Yu. Yu.,Shchadneva, N. A.
, p. 1228 - 1235 (2020/10/02)
Abstract: Methyl N-alkyl-, N-cycloalkyl-, and N-arylcarbamates were synthesized by reaction of the correspondingamines with dimethyl carbonate in the presence of binder-free FeHY zeolite. Theoptimal conditions (reactant ratio, amount of the catalyst, temperature,reaction time) were found to afford the target products with high yields.
Preparation of Methyl Carbamates from Primary Alkyl- and Arylcarboxamides Using Hypervalent Iodine
Moriarty, Robert M.,Chany, Calvin J.,Vaid, Rahde K.,Prakash, Om,Tuladhar, Sudersan M.
, p. 2478 - 2482 (2007/10/02)
A series of 14 primary alkyl- and arylcarboxamides were treated with PhI(OAc)2 in KOH-CH3OH at 5-10 deg C to give the corresponding methyl carbamates in good to excellent yields.These conditions avoid the use of elemental bromine or heavy metal reagents (Pb(OAc)4, AgOAc, Hg(OAc)2), while taking advantage of the commercial availability of PhI(OAc)2.The methyl carbamates are easily purified via column chromatography on silica gel.The isolated yields of the carbamates ranged from 72percent for methyl N-cyclopropylcarbamate to 97percent for methyl N-phenylcarbamate.
