Methanol → HCID 22259533, compound

HRID 1901144Notes

Reaction equation

HRID 1901144 reaction equation
[C:1]([O:6][CH3:7])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:8]([O:13][CH2:14][CH:15]1[O:17][CH2:16]1)(=[O:12])[C:9]([CH3:11])=[CH2:10].N(C(C)(CC)C([O-])=O)=NC(C)(CC)C([O-])=O.CO>C1(C)C=CC=CC=1>[C:1]([O:6][CH3:7])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:8]([O:13][CH2:14][CH:15]1[O:17][CH2:16]1)(=[O:12])[C:9]([CH3:11])=[CH2:10]

Participants

6

Conditions

Temperature
80 °C

Procedure

To a solution of methyl methacrylate (50.1 g, 0.5 mole) and glycidyl methacrylate (28.4 g, 0.2 mole) in toluene (240 ml), 2,2'-azobis(methyl 2-methylpropionate) (0.8 g) was added, then the mixture was reacted with stirring at 80° C. for 7 hours under nitrogen. After cooling, the reaction mixture was poured into methanol (200 ml) and the polymer was precipitated. The polymer was filtered and dried under reduced pressure to give 77 g of poly(methyl methacrylate/glycidyl methacrylate) as white powders having Mw 35800 and Mn 19200 (GPC with polystyrene calibration). The composition of the polymer was found to be methyl methacrylate unit and glycidyl methacrylate unit in molar ratio of ca. 5:2 based on 1HNMR analysis.

Workup

  1. customthe mixture was reacted
  2. temperatureAfter cooling
  3. customthe polymer was precipitated
  4. filtrationThe polymer was filtered
  5. customdried under reduced pressure

Sources & evidence

ORD record
ord-3b16fa51801e463b969205b0bcba4776
Source dataset
uspto-grants-1996_11
Patent number
US05576359

Reaction notes

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