HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → N-(Butoxycarbonylethyl)Maleimide Styrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Maleimide styrene | HCID 66643759 | — |
| Reactant | N-ethoxycarbonyliminocarbamate | HCID 86599450 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(Butoxycarbonylethyl)Maleimide Styrene | HCID 86751013 | — |
Reaction Steps
2 g of maleimide-styrene copolymer are dissolved in 25 ml of DMF, 3 g of triphenylphosphine and 1.8 ml of ethyl azodicarboxylate are added, and the mixture is stirred for 15 minutes, during which slight warming occurs. 1.5 ml of L-(-)-butyl lactate are then added, and the mixture is stirred at room temperature for 20 hours, giving a clear, red-brown solution, which is poured into 300 ml of methanol. A milky-white precipitation of the polymer is obtained. Since the substance has a tacky consistency, it is separated off by centrifugation. After repeated washing with methanol and centrifugation, the product is dried at 70° C. in a drying cabinet. Yield 2.5 g. The polymer exhibits a rotation value of [α]D20 =+6.7° in the DMF solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05644016 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-5ae181e1de3a4fe1ac280fea4242498b |
| Source note | uspto-grants-1997_07 |