Water → Dodecyl 2-methylprop-2-enoate--methyl 2-methylprop-2-enoate (1/1)

HRID 1698933Notes

Reaction equation

HRID 1698933 reaction equation
C(OS(C1C=CC=CC=1)(=O)=O)CCCCCCCCCCC.[Na].O.[C:25]([O:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42])(=[O:29])[C:26]([CH3:28])=[CH2:27]>C(OC)(=O)C(C)=C.N(C(C)(CC(C)C)C#N)=NC(C)(CC(C)C)C#N>[C:25]([O:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH3:42])(=[O:29])[C:26]([CH3:28])=[CH2:27].[C:25]([O:30][CH3:31])(=[O:29])[C:26]([CH3:28])=[CH2:27]

Participants

6

Procedure

In a mixed solution of 75 parts of dodecyl methacrylate and 25 parts of methyl methacrylate there was dissolved 0.1 part of 2,2′-azobis(2,4-dimethylvaleronitrile). To this there was then added a mixed solution containing 2.0 parts of sodium dodecylbenzenesulfonate and 300 parts of distilled water, and after stirring for 4 minutes at 10,000 rpm with a homomixer, it was passed twice through a homogenizer at 30 MPa pressure to obtain a stable dodecyl methacrylate/methyl methacrylate preliminary dispersion. This was charged into a separable flask equipped with a stirring blade, condenser, thermocouple and nitrogen inlet, the internal temperature was raised to 80° C. under a nitrogen stream and the mixture was stirred for 3 hours for radical polymerization, to obtain a dodecyl methacrylate/methyl methacrylate copolymer particle dispersion (hereunder referred to as “B-4”).

Workup

  1. additionTo this there was then added a mixed solution

Sources & evidence

ORD record
ord-706063f44a924d98985d91c56ebf40a3
Source dataset
uspto-grants-2002_02
Patent number
US06344493B2

Reaction notes

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