Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764543Generated: October 31, 2026

Acrylonitrile → Acrylonitrile

https://huagongshe.com/reaction/1764543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantIsobutyleneHCID 8255—
ProductAcrylonitrileHCID 7855—
ProductIsobutyleneHCID 8255—
Product5-MethylenenonanedinitrileHCID 3016531—
Product5-Methylnon-4-enedinitrileHCID 53899731—

Reaction Steps

Referring now to the drawing, an embodiment involving a continuous process for the reaction of acrylonitrile, isobutylene and a monoadduct of acrylonitrile and isobutylene to produce 5-methylenenonanedinitrile and 5-methyl-4-nonenedinitrile will be described. Acrylonitrile and isobutylene are introduced into single-stage reactor 11 by way of conduit means 12 and 13, respectively. A monoadduct of acrylonitrile and isobutylene, i.e. predominately 5-methyl-5-hexenenitrile with a small amount of 2,4-dimethyl-4-pentenenitrile, is introduced into reactor 11 by way of conduit means 14, while water is introduced into reactor 11 by way of conduit means 15. A convenient method of carrying out the production of the diadduct in reactor 11 comprises heating the mixture of acrylonitrile, isobutylene, and the mixture of 5-methyl-5-hexenenitrile and 2,4-dimethyl-4-pentenenitrile in a reaction pressure vessel at a temperature within the range of about 240° to about 350° C. and at pressures in the range of about 3.45 to about 27.58 MPa (about 500 to about 4000 psig), the mol ratio of the acrylonitrile to the isobutylene being in the range of about 5:1 to about 0.2:1, and the concentration of the monoadduct reactant in the reaction mixture being in the range of about 20 to about 80 weight percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04117002
Source datasetuspto-grants-1978_09
ORD IDord-b830b847306e47a583f6e79f36df498c
Source noteuspto-grants-1978_09