Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 2,2'-Azobis[2-(2-imidazolin-2-yl)propane] dihydrochloride | HCID 9949101 | — |
| Reactant | 2-Propenamide, N-(3-aminopropyl)-2-methyl-, hydrochloride (1:1) | HCID 10375005 | — |
| Reactant | Allyl alpha-D-mannopyranoside | HCID 11183597 | — |
| Solvent | Water | HCID 962 | — |
| Product | Demannose | HCID 161658 | — |
Reaction Steps
A 40 mol % mannose polymer was prepared as follows. Allyl α-D-mannopyranoside (1.77 g, 8.0 mmol), 2-hydroxyethylacrylate (1.36 g, 11.7 mmol), N-(3-aminopropyl)methacrylamide hydrochloride (89.6 mg, 0.5 mmol) and 2,2′-Azobis-[2-(2-imidazolin-2-yl)-propane]dihydrochloride (23.7 mg, 0.073 mmol) were added into a 50 ml round bottom flask, followed by addition of water (28.8 ml). The mixture was dissolved under magnetic stirring at room temperature. After purging with nitrogen for 5 min, the mixture was heated to 60° C. and polymerized at that temperature for 12 hours. Upon cooling a slightly yellow and viscous solution was obtained. This solution was dialysed (25 k MWCO regenerated cellulose) overnight against water, and freeze-dried to obtain a white fluffy polymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691517B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-3e39440e2b3a4c0d8abc4fda76a9d008 |
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| Source note | uspto-grants-2014_04 |
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