戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6034作成日:2026年10月24日

4-Nitrophenol → 4-nitrophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranoside

https://huagongshe.com/ja/reaction/6034

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrophenolHCID 980—
反応物2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
触媒ZincchlorideHCID 3007855—
触媒Silver imidazolateHCID 10931941—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物4-nitrophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506784825.2%

反応条件

温度50 °C

反応手順

A suspension of 5.6 g (15.8.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 2 g (14.3.10-3 mol) of 4-nitrophenol, 4 g (29.3.10-3 mol) of zinc chloride and 3.8 g (21.7.10-3 mol) of silver imidazolate in 80 ml of anhydrous methylene chloride is stirred at 50° C., under an inert atmosphere, in the absence of light and in the presence of a molecular sieve (400 pm). After 48 h at this temperature, the reaction mixture is filtered on Celite®, washed with a 1N aqueous solution of hydrochloric acid, then a 1N solution of sodium hydroxide and finally water and dried over magnesium sulfate (MgSO4). After evaporation to dryness, the residue is purified by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 v/v) as the eluent. 1.5 g (yield: 25%) of the expected product are obtained by precipitation in ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246961
出典データセットuspto-grants-1993_09
ORD IDord-b9a267834ffc4d2eb782eaa76b1e6127
出典メモuspto-grants-1993_09