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ChemicalBook CAS DataBase List N-Methyl-2-pyrrolidone

N-Methyl-2-pyrrolidone synthesis

14synthesis methods
1-Methyl-2-pyrrolidinone is manufactured by the reaction of buytrolactone with methylamine (Hawley 1977). Other processes include preparation by hydrogenation of solutions of maleic or succinic acids with methylamine (Hort and Anderson 1982). Manufacturers of this chemical include Lachat Chemical, Inc, Mequon, Wisconsin and GAF Corporation, Covert City, California.
-

Yield:872-50-4 99.9%

Reaction Conditions:

in water at 300; under 75007.5 Torr;Concentration;

Steps:

1.3

A methylamine aqueous solution F3 and γ-butyrolactone F1 in provided to the continuous reactor R, and the 300 °C temperature and 100 the reaction under pressure, low liquid hourly space velocity (LHSV) is 1.0. The reactor R through a separator after S, generated by this N-methyl pyrrolidone F4 and water F4 are separated from each other. The separated water F6 through one or a plurality of in the 200 °C temperature and 40 the operation of the separator under pressure to collect, and with a methylamine F2 the circulation enters reactor R again is mixed in an aqueous solution of methylamine of F3. Γ-butyrolactone with respect to to 1.01 provide excess of the molar ratio of the a methylamine. Conversion and yield (dependent upon the reactant concentration of a methylamine (MMA)) as shown in table 1 is shown in

References:

CN105906542,2016,A Location in patent:Paragraph 0037; 0038; 0042

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