戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 850693作成日:2026年10月26日

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

https://huagongshe.com/reaction/850693

反応式

関与物質

役割名称HCID仕込み量
反応物SucroseHCID 5988—
反応物Glycidyl acrylateHCID 7836—
反応物4-MethoxyphenolHCID 9015—
反応物AluminumHCID 5359268—
溶媒PhosphateHCID 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-enoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06018033
出典データセットuspto-grants-2000_01
ORD IDord-00c5568940204401afab0faf8b41193f
出典メモuspto-grants-2000_01