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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66451Generated: October 26, 2026

Azobisisobutyronitrile → Butadiene maleic acid

https://huagongshe.com/reaction/66451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant1,3-ButadieneHCID 7845—
ReactantMaleic AnhydrideHCID 7923—
Reactant1-DodecanethiolHCID 8195—
ReactantSodium HydroxideHCID 14798—
ReactantSulfurHCID 5362487—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductButadiene maleic acidHCID 86738509—

Reaction Steps

A polymerization was carried out at 70° C. for 6 hrs. using 54.1 g. of butadiene, 98.1 g. of maleic anhydride, 1.7 g. of azobisisobutyronitrile and 36.0 g. of n-dodecylmercaptan in 750 cc. of acetone. There was obtained 61.0 g. of a white copolymer with an intrinsic viscosity of 0.08. Proportion of the end dodecylthio group in the copolymer was found by the elementary analysis for sulfur to be 5.4%. A reaction was carried out at 80° C. for 1 hr. using 16.1 g. of the copolymer, 6.0 g. of sodium hydroxide and 139 g. of water to give an aqueous solution of a butadiene-maleic acid copolymer sodium salt containing end dodecylthio groups. A composition identical in composition with the composition of Example 2 was prepared using the above-prepared aqueous solution, an aqueous calcium chloride solution at a concentration of 0.1 M/l, an aqueous solution of sodium lauryl sulfate at a concentration of 30% and water to which THPA was added in the same amount as that of the copolymer salt. Aqueous gel obtained from the composition was slower in rate of the gelation and lower in strength of the gel as compared with the aqueous gel of Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342665
Source datasetuspto-grants-1982_08
ORD IDord-612335c55f524cf5863308144335608a
Source noteuspto-grants-1982_08