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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703742Generated: November 1, 2026

Azobisisobutyronitrile → HCID 173649, compound

https://huagongshe.com/reaction/1703742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantMaleic AnhydrideHCID 7923—
Reactant1-HexeneHCID 11597—
SolventMethanolHCID 887—
ProductHCID 173649HCID 173649—

Reaction Steps

A separable flask fitted with a reflux condenser was charged with 98 parts of maleic anhydride, 300 parts of methyl ethyl ketone, 84 parts of hexene-1 and 4 parts of azobisisobutyronitrile, and the mixture was reacted with stirring in an atmosphere of nitrogen at 65°-70° C. After carrying out the reaction for 10 hours, the system was cooled to room temperature and cold methanol was added to precipitate a polymer, which was separated, collected and dried under reduced pressure to obtain 108 parts of a hexene-1-maleic anhydride copolymer (mol ratio 1:1, MW = 3800). A mixture of 91 parts of the so obtained copolymer and 400 parts of a 10% aqueous sodium hydroxide solution was stirred at 80°-90° C. to obtain an aqueous solution of a water-soluble hexene-1-sodium maleate copolymer (hereinafter referred to as water-soluble salt (II-2) or Na salt of (C6 -MA) copolymer).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125410
Source datasetuspto-grants-1978_11
ORD IDord-4cbc0b6dd5984b13bb62b12e808baf50
Source noteuspto-grants-1978_11