N-vinyl-2-pyrrolidone → HCID 86734509, compound
Reaction equation
[CH:1]([N:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[O:8])=[CH2:2].[CH:9]([CH:11]=[CH2:12])=[O:10]>O>[CH:1]([N:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[O:8])=[CH2:2].[CH:9]([CH:11]=[CH2:12])=[O:10]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 3-neck, round bottom flask equipped with a mechanical stirrer, means for maintaining an inert atmosphere in the flask and a thermometer is charged with 368 ml. of distilled water, 22.2 g. (0.2 mol) N-vinyl pyrrolidone and 1.3 g. (0.02 mol) of acrolein. The flask is flushed with nitrogen, and the contents of the flask are maintained under nitrogen during the course of the reaction. The mixture is stirred, the temperature is raised to 50°-55° C. and maintained at this temperature, and 0.2 g. of 4,4'-azobiscyanopentanoic acid is added. After 2 hours reaction an additional 0.2 g. of 4,4'-azobiscyanopentanoic acid is added, and the reaction is allowed to continue for an additional 3 hours. At the end of this time, the mixture is filtered to remove a small amount of insoluble material. The filtrate obtained contains about 6 percent by weight of copolymer. The solution may be used as such or isolated by spray or drum drying.
Workup
- customA 3-neck, round bottom flask equipped with a mechanical stirrer
- temperaturefor maintaining an inert atmosphere in the flask
- additiona thermometer is charged with 368 ml
- customThe flask is flushed with nitrogen
- temperaturethe contents of the flask are maintained under nitrogen during the course of the reaction
- temperaturethe temperature is raised to 50°-55° C.
- temperaturemaintained at this temperature, and 0.2 g
- additionof 4,4'-azobiscyanopentanoic acid is added
- customAfter 2 hours reaction an additional 0.2 g
- filtrationAt the end of this time, the mixture is filtered
- customto remove a small amount of insoluble material
- customThe filtrate obtained
- customisolated by spray or drum
- customdrying
Sources & evidence
- ORD record
- ord-a5d0e819e6314ff9bd9652dfddb52006
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04009313
Reaction notes
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