Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylborane | HCID 7357 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | N-Methyl-N-vinylacetamide | HCID 18530 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | HCID 53935447 | HCID 53935447 | — |
| Solvent | tert-Butyl hydroperoxide | HCID 6410 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 86741582 | HCID 86741582 | — |
Reaction Steps
Copoly(N-methyl-N-vinylacetamide/maleic anhydride) was prepared as follows. About 5 g of maleic anhydride free of maleic acid was dissolved in about 32 g of tetrahydrofuran. This solution was placed in a flask fitted with a dropping funnel, mechanical stirrer and nitrogen inlet. The dropping funnel was charged with about 4 g of N-methylvinylacetamide dissolved in about 13 g of tetrahydrofuran and 0.25 ml of 90% t-butyl hydroperoxide. The temperature of the reaction was adjusted to about 30° C., and the N-methyl-N-vinylacetamide solution was added dropwise over a period of about 4 hours. About 0.5 ml of a 1 Molar solution of triethylborane in hexane was added to the reaction flask at the beginning of the reaction run, and every hour thereafter. At the end of about 7 hours reaction time, the product polymer was precipitated by addition of about 50 ml of petroleum ether. Ths slurry was filtered and washed with diethylether and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04673508 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-20dd3c9e996846798f5585a63a58e8ec |
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| Source note | uspto-grants-1987_06 |
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