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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66450Generated: October 27, 2026

Azobisisobutyronitrile → Butadiene maleic acid

https://huagongshe.com/reaction/66450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant1,3-ButadieneHCID 7845—
ReactantMaleic AnhydrideHCID 7923—
ReactantSodium HydroxideHCID 14798—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventCyclohexanoneHCID 7967—
ProductButadiene maleic acidHCID 86738509—

Reaction Steps

A polymerization was carried out at 70° C. for 4 hours using 54.1 g. of butadiene, 98.1 g. of maleic anhydride and 1.7 g. of azobisisobutyronitrile in 750 cc. of acetone. There was obtained 106.0 g. of a pale yellow copolymer with an intrinsic viscosity of 0.50 as measured in cyclohexanone at 30° C. (All measurements are done hereinbelow under the same conditions.) A reaction was carried out at 80° C. for 1 hour using 15.2 g. of the copolymer, 6.0 g. of sodium hydroxide and 131 g. of water to form an aqueous solution of butadiene-maleic acid copolymer sodium salt. The aqueous solution, an aqueous calcium-chloride solution at a concentration of 0.1 M/l, 30% aqueous solution of sodium lauryl sulfate (LAS) and water were employed together with THPA in an amount equal to the copolymer salt to prepare compositions shown in Table 1. Whereas aqueous gel was formed with the compositions of Examples 1-5, no aqueous gel was formed or the polymer was precipitated with the compositions of Comparative Examples 1-3, in which one of the essential components was not contained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342665
Source datasetuspto-grants-1982_08
ORD IDord-78175b1f1a94416494e08d65214ac9e3
Source noteuspto-grants-1982_08