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N-vinylpyrrolidone-vinyl acetate glycidyl acrylate → N-vinyl-2-pyrrolidone

HRID 1089656
Notes
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Reaction equation

HRID 1089656 reaction equation
[C:1]([O:4][CH:5]=[CH2:6])(=[O:3])[CH3:2].[CH:7]([N:9]1[CH2:13][CH2:12][CH2:11][C:10]1=[O:14])=[CH2:8].[C:15]([O:19][CH2:20][CH:21]1[O:23][CH2:22]1)(=[O:18])[CH:16]=[CH2:17]>C(O)C>[CH:7]([N:9]1[CH2:13][CH2:12][CH2:11][C:10]1=[O:14])=[CH2:8].[C:1]([O:4][CH:5]=[CH2:6])(=[O:3])[CH3:2].[C:15]([O:19][CH2:20][CH:21]1[O:23][CH2:22]1)(=[O:18])[CH:16]=[CH2:17]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 1

HCID 86745368N-vinylpyrrolidone-vinyl acetate glycidyl acrylate

Product 3

HCID 6917N-vinyl-2-pyrrolidoneHCID 7836Glycidyl acrylateHCID 7904Vinyl Acetate

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A hydrophilic coating was formed by the same method as that of Example 3 except using N-vinylpyrrolidone-vinyl acetate-glycidyl acrylate copolymer having a molecular weight of about 500,000 obtained by polymerizing 7.0 g of N-vinylpyrrolidone, 2.0 g vinyl acetate and 1.0 g of glycidyl acrylate in ethyl alcohol by using V-65 (azobisvaleronitrile) as an initiator as a component B.

Workup

  1. customA hydrophilic coating was formed by the same method as that of Example 3

Sources & evidence

ORD record
ord-99835f1872314b45901cf90a9baceaa8
Source dataset
uspto-grants-1992_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05079093

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes