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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260135Generated: November 1, 2026

Maleic Anhydride → HCID 18995304, compound

https://huagongshe.com/reaction/260135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantHCID 15789584HCID 15789584—
CatalystPhosphoric AcidHCID 1004—
SolventDimethylformamideHCID 6228—
SolventO-XyleneHCID 7237—
ProductHCID 18995304HCID 1899530496.7%

Reaction Steps

In the same reactor used in Example 2A, there were placed 26.5 g (0.27 mole) of maleic anhydride, 0.7 g of phosphoric acid and 150 ml of mixed xylene. A solution was then added dropwise thereto under reflux of xylene, the solution having been prepared by thermally dissolving 52.8 g (0.1 mole) of 1,4-bis[4(4-aminophenoxy),α,α-dimethylbenzyl)benzene obtained in Example 1A in a mixture of 100 ml of mixed xylene and 50 ml of N,N-dimethylformamide. A dropping time of 5 hours and an aging time of 2 hours were used in order to carry out the reaction. The reaction solution was concentrated to about 1/2 the original amount and then cooled. When a temperature of 80° C. had been reached; 50 g of water was added thereto. Afterward, the solution was slowly cooled with stirring, so that crystals were precipitated. The crystals were then cooled to room temperature, filtered, and washed with cold methanol. 66.5 g of desired crude 1,4-bis[4-(4-maleimidophenoxy)-α, α-dimethylbenzyl]benzene was obtained. Its yield was 96.7%, and its purity according to HLC was 97.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05525704
Source datasetuspto-grants-1996_06
ORD IDord-469fde6654344f6eadd2f2ff7241ef5a
Source noteuspto-grants-1996_06