HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15055049, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 67785823 | HCID 67785823 | — |
| Product | HCID 15055049 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04939070 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-ddb574c7b48a4aca965644c89c39dd5a |
| Source note | uspto-grants-1990_07 |