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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165032Generated: October 31, 2026

Acetic Anhydride → HCID 15055049, compound

https://huagongshe.com/reaction/2165032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantMaleic AnhydrideHCID 7923—
ReactantSodium AcetateHCID 517045—
ReactantHCID 67785823HCID 67785823—
ProductHCID 15055049HCID 15055049—

Reaction Steps

The poly(N-(4-tert-butyloxycarbonyloxyphenyl) maleimide is synthesized according to the following scheme. Di-t-butylpyrocarbonate is reacted with p-aminophenol to give p-(t-butyloxycarbonyloxy) aniline, I. Reaction of I with maleic anhydride then affords N-(p-t-butyloxycarbonyloxyphenyl)maleamic acid, II. Monomer II is modified by treatment with sodium acetate and acetic anhydride to yield monomer III, N-(p-t-butyloxycarbonyloxyphenyl)maleimide. Monomer III is polymerized in the presence of azoisobutylnitrile (AIBN) to yield poly-N-(4-tert-butyloxycarbonyloxyphenyl) maleimide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939070
Source datasetuspto-grants-1990_07
ORD IDord-ddb574c7b48a4aca965644c89c39dd5a
Source noteuspto-grants-1990_07