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HRID 6029作成日:2026年10月24日

4-Cyanophenol → 4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranoside

https://huagongshe.com/ja/reaction/6029

反応式

関与物質

役割名称HCID仕込み量
反応物4-CyanophenolHCID 13019—
反応物2,3,4-Tri-o-acetyl-5-thioxylopyranosyl bromideHCID 11382683—
触媒Zinc OxideHCID 3007857—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
生成物4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506784635%

反応条件

温度50 °C

反応手順

A suspension of 0.5 g (1.4.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-D-xylopyranosyl bromide, 0.25 g (2.1.10-3 mol) of 4-hydroxybenzonitrile and 170 mg (2.1.10-3 mol) of zinc oxide (ZnO) in 4 ml of anhydrous toluene and 4 ml of acetonitrile is stirred at 50° C., under an inert atmosphere, in the presence of a molecular sieve (1 nm), for 48 h. The reaction medium is subsequently filtered on Celite® in ethyl acetate and then washed with a 1N aqueous solution of hydrochloric acid, water, a 1N solution of sodium hydroxide and then a saturated solution of NaCl. The solution obtained is dried over sodium sulfate and the solvent is evaporated off under reduced pressure. The residue obtained is purified by chromatography on silica gel using a hexane/ethyl acetate mixture (2/1 v/v) as the eluent to give 194 mg (yield: 35%) of the expected product.

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-e7b03201d99f4d3da974587d2d9e325c
出典メモuspto-grants-1993_09