Styrene → Prop-2-enenitrile--ethenylbenzene (1/1)

HRID 1904806Notes

Reaction equation

HRID 1904806 reaction equation
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9](#[N:12])[CH:10]=[CH2:11].C(S)CCCCCCCCCCC>>[CH2:11]=[CH:10][C:9]#[N:12].[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Participants

4

Procedure

A graft precursor was prepared by following the procedure of Example 13, except that a mixed monomer consisting of 210 g of styrene, 90 g of acrylonitrile, and 0.6 g of n-dodecyl mercaptan as a molecular weight regulator was used in the place of 300 g of styrene. Separately, an acrylonitrile-styrene copolymer was obtained by placing a mixed solution consisting of 70 g of styrene, 30 g of acrylonitrile, 0.2 g of n-dodecyl mercaptan, and 0.5 g benzoyl peroxide in 500 g of an aqueous 1% polyvinyl alcohol solution and holding the resultant mixture at a temperature of 80° to 85° C. for seven hours to complete polymerization. Graft resin compositions were produced by following the procedure of Example 13, except that the amounts of the copolymer, the graft precursor mentioned above, the propylene polymer to be mixed were varied as indicated in Table 7. The results were as shown in Table 7.

Workup

  1. customA graft precursor was prepared

Sources & evidence

ORD record
ord-b2265d40bb0143b98ca940f20d20198d
Source dataset
uspto-grants-1989_06
Patent number
US04839423

Reaction notes

Loading…