Azobisisobutyronitrile → 3,6-Dimethyl-3-octanol

HRID 234868

Reaction equation

HRID 234868 reaction equation
C(O[CH2:7][C:8]1[CH:13]=[CH:12]C=[CH:10][CH:9]=1)(=O)C(C)=C.[C:14]([OH:18])(=O)[CH:15]=[CH2:16].S[CH2:20]CC(OC)=O.N(C(C1CC1)(C)C#N)=NC(C1CC1)(C)C#N.N(C(C)(C)C#N)=NC(C)(C)C#N>>[CH3:10][CH2:9][CH:8]([CH2:13][CH2:12][C:14]([OH:18])([CH2:15][CH3:16])[CH3:20])[CH3:7]

Participants

6

Procedure

To the solution was dropwise added a mixed solution of 85.0 g of benzyl methacrylate, 15.0 g of acrylic acid, 2.0 g of methyl 3-mercaptopropionate and 1.2 g of 2,2'-azobis(2-cyclopropylpropionitrile) (abbreviated as ACPP) over a period of one hour, followed by stirring for one hour. To the reaction mixture was added 0.8 g of ACPP, followed by reacting for 2 hours. Further, 0.5 g of 2,2'-azobis(isobutyronitrile) (abbreviated as AIBN) was added thereto, the reaction temperature was adjusted to 80° C., and the reaction was continued for 3 hours. After cooling, the reaction mixture was passed through a nylon cloth of 200 mesh to obtain a white dispersion which was a latex of good monodispersity with a polymerization rate of 97% and an average grain diameter of 0.17 μm. The grain diameter was measured by CAPA-500 manufactured by Horiba Ltd. (hereinafter the same).

Workup

  1. additionTo the reaction mixture was added 0.8 g of ACPP
  2. waitby reacting for 2 hours
  3. customwas adjusted to 80° C.
  4. waitthe reaction was continued for 3 hours
  5. temperatureAfter cooling
  6. customto obtain a white dispersion which

Sources & evidence

ORD record
ord-478f258913fe49559bfe67d68cad9336
Source dataset
uspto-grants-1997_01
Patent number
US05597672

Linked notes

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