HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576741Generated: October 30, 2026
Maleic Anhydride → Furan-2,5-dione--2-methylprop-1-ene (1/1)
https://huagongshe.com/reaction/1576741
Participants
| Role | Name | HCID | Charge |
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| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Product | Furan-2,5-dione--2-methylprop-1-ene (1/1) | HCID 161524 | — |
Reaction Steps
Following the general procedure of Example 2 equimolar proportions of isobutylene and maleic anhydride were copolymerized in a pressure reactor employing a peroxide catalyst to produce an isobutylene-maleic anhydride copolymer which was found to have a molecular weight of about 7,000,000. 9 Grams of said copolymer was dissolved in 41 grams of N-methylpyrrolidone and a solution of 0.09 gram of diethylene glycol in 4 grams of N-methylpyrrolidone was added thereto to produce a spinning dope containing 16.6% by weight of the copolymer and 1% by weight of said copolymer of the diethylene glycol cross-linking agent. when the solution was homogeneous, it was forced under a pressure of 70 pounds per square inch through a 15 hole spinnerette of 3 mil thickness into a coagulation bath of water at a temperature of 23°C. The resulting fiber was collected from the coagulation bath and placed in an oven at 105°C. for one hour to complete drying and solvent stripping from the fibers and to accomplish the cross-linking reaction. The fibers were then placed in a pressure vessel at room temperature and treated with gaseous ammonia at a pressure of 20 p.s.i. for 1 hour. The resulting fiber product was determined to have a gel capacity of 406 grams per gram in distilled water and 35 grams per gram in 0.27 N sodium chloride solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03983095 |
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| Source dataset | uspto-grants-1976_09 |
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| ORD ID | ord-24808fecb6334114a87fcd30300d8406 |
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| Source note | uspto-grants-1976_09 |
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