Methyl Methacrylate → HCID 131711038, compound
Reaction equation
[C:1]([O:6][CH3:7])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:8]([O-:13])(=[O:12])[C:9]([CH3:11])=[CH2:10].[CH2:14]([Sn+:18]([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:19][CH2:20][CH2:21][CH3:22])[CH2:15][CH2:16][CH3:17].C([O-])(=O)C(C)=C.[CH2:33]([Sn+:36]([CH2:40][CH2:41][CH3:42])[CH2:37][CH2:38][CH3:39])[CH2:34][CH3:35].C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C1C=CC=CC=1>[C:1]([O-:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH2:23]([Sn+:18]([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:19][CH2:20][CH2:21][CH3:22])[CH2:24][CH2:25][CH3:26].[CH3:35][CH2:34][CH2:33][Sn:36]([O:12][C:8]([C:9]([CH3:11])=[CH2:10])=[O:13])([CH2:40][CH2:41][CH3:42])[CH2:37][CH2:38][CH3:39].[C:1]([O:6][CH3:7])(=[O:5])[C:2]([CH3:4])=[CH2:3]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
The monomers of P51 were first synthesized. Tri-n-butyltin methacrylate was prepared as was tripropyltin methacrylate. These esters were isolated as crystals from petroleum ether. Methyl methacrylate was uninhibited. All uninhibited monomers were refrigerated below 40° F when stored for short periods of time. Tri-n-butyltin methacrylate (0.4 mole), tri-n-propyltin methacrylate (0.4 mole) and methyl methacrylate (0.4 mole) were reacted in 300 ml of benzene using benzoyl peroxide (0.5% by weight) as initiator. The reaction mixture was refluxed for 24 hours in a 1-liter, 3-necked resin flask equipped with a reflux condenser, a thermometer, such that it read the temperature of the reactants and a mechanical stirrer. The resultant polymer was clear and could be cast as a film from the benzene solution. Analysis showed 29.35% Sn.
Workup
- customwere refrigerated below 40° F
- waitstored for short periods of time
- temperatureThe reaction mixture was refluxed for 24 hours in a 1-liter, 3-necked resin flask
- customequipped with a reflux condenser
Sources & evidence
- ORD record
- ord-f21cabc8453742959013ac1fc37bda93
- Source dataset
- uspto-grants-1978_02
- Patent number
- US04075319
Reaction notes
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