化工社化工社 化学情報印刷レポート · 研究参考用
Sucrose → (2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol;prop-2-enoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sucrose | HCID 5988 | — |
| 反応物 | Glycidyl acrylate | HCID 7836 | — |
| 反応物 | 4-Methoxyphenol | HCID 9015 | — |
| 反応物 | Aluminum | HCID 5359268 | — |
| 溶媒 | Phosphate | HCID 1061 | — |
| 生成物 | (2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol;prop-2-enoate | HCID 131721615 | — |
反応手順
Four batches of sucrose acrylate monomers were prepared. For each batch, 10 g of sucrose, 1.9 g of TAB (99%), and a small amount of p-methoxyphenol, which was used as a polymerization inhibitor, were dissolved in 20 ml phosphate buffered aqueous solution (pH 7.2, 0.05 M) in a 200 ml Erlenmeyer flask equipped with magnetic stirrer. The TAB was used as a phase transfer catalyst. Glycidyl acrylate (GA) (Lancaster Synthesis, Inc.; Windham, N.H.) was added to each batch to make sucrose:GA ratios of 1:4, 1:1.5, 1:1:5, and 1:8. The reaction was performed at room temperature with continuous stirring and the flasks were covered with aluminum foil to avoid the light.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06018033 |
| 出典データセット | uspto-grants-2000_01 |
| ORD ID | ord-00c5568940204401afab0faf8b41193f |
| 出典メモ | uspto-grants-2000_01 |