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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6029Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-CyanophenolHCID 13019—
Edukt2,3,4-Tri-o-acetyl-5-thioxylopyranosyl bromideHCID 11382683—
KatalysatorZinc OxideHCID 3007857—
LösungsmittelTolueneHCID 1140—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506784635%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246961
Quelldatensatzuspto-grants-1993_09
ORD IDord-e7b03201d99f4d3da974587d2d9e325c
Quellennotizuspto-grants-1993_09