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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6029생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물4-CyanophenolHCID 13019—
반응물2,3,4-Tri-o-acetyl-5-thioxylopyranosyl bromideHCID 11382683—
촉매Zinc OxideHCID 3007857—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
생성물4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506784635%

반응 조건

온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-e7b03201d99f4d3da974587d2d9e325c
출처 메모uspto-grants-1993_09