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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616004Generated: October 30, 2026

Azobisisobutyronitrile → HCID 86735441, compound

https://huagongshe.com/reaction/616004

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
ReactantCyclohexanoneHCID 7967—
ReactantPenta-1,3-dieneHCID 15301—
SolventTolueneHCID 1140—
ProductHCID 86735441HCID 86735441—

Reaction Steps

of piperylene, 98g. of maleic anhydride, 1.6g. of azobisisobutyronitrile and 500 ml of cyclohexanone were fed in a 1 liter autoclave and a polymerization conducted for 2 hours at 80° C. under a nitrogen atmosphere. The resulting viscous polymerized solution was introduced in 5 liter of toluene to allow the copolymer to be deposited. The precipitates were collected by means of filtration, washed with toluene several times and dried under reduced pressure. As a result, there was obtained a purified piperylene-maleic anhydride copolymer in 35% (59g.) yield, which had an intrinsic viscosity of 0.42 determined in dimethylformamide at 30° C. 20g. of the copolymer, 13.5g. of potassium hydroxide and 400 ml. of water were fed in a separable 1 liter flask equipped with a cooler and a stirrer, and stirring was then applied for 1 hour at 100° C. under a nitrogen gas stream, to give a homogeneous aqueous solution with a pH of 12. A half amount of the aqueous solution was withdrawn into an Erlenmeyer flask and the pH thereof was brought down to 7.5 using an aqueous sulfuric acid solution. To the other aqueous solution without pH adjustment was added, little by little with continued stirring, a separately prepared aqueous solution consisting of 11g. of magnesium chloride hexahydrate and 200 ml. of water. To the pH adjusted one was added at a time 11g. of a solid magnesium choride hexahydrate and stirring was applied for 1 hour. After these operations, both aqueous solutions became whitely turbid and therefore they were left standing for 2 hours at room temperature. As a result, both were each separated into two liquid layers. Removal of the respective upper layers left viscous aqueous solutions of the respective lower layers, which on heating were converted into rubber-like solids and on cooling reverted to their original states of aqueous solutions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04072646
Source datasetuspto-grants-1978_02
ORD IDord-0347c6810d9742e583632e75a1d9631c
Source noteuspto-grants-1978_02