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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5992생성일: 2026년 10월 23일

4-Thiobenzonitrile → 4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside

https://huagongshe.com/ko/reaction/5992

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참여 물질

역할이름HCID투입량
반응물4-ThiobenzonitrileHCID 585058—
반응물2,3,4-Tri-o-acetyl-5-thioxylopyranosyl bromideHCID 11382683—
촉매ZincchlorideHCID 3007855—
촉매Silver imidazolateHCID 10931941—
용매AcetonitrileHCID 6342—
생성물4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479533217%

반응 조건

온도50 °C

반응 단계

A suspension of 625 mg (1.76.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-D-xylopyranosyl bromide, 200 mg (1.48.10-3 mol) of 4-mercaptobenzonitrile and a 400 pm molecular sieve in 10 ml of acetonitrile is stirred in the presence of 605 mg (4.4.10-3 mol) of zinc chloride and 310 mg (1.8.10-3 mol) of silver imidazolate, in the absence of light, under an inert atmosphere. After heating at 50° C. for 3 h, the reaction mixture is filtered on Celite® in ethyl acetate. The filtrate is washed with a 1N solution of hydrochloric acid, water, a 1N solution of sodium hydroxide, water and finally a saturated solution of sodium chloride, dried over magnesium sulfate and evaporated under reduced pressure. After purification by chromatography on silica gel using a hexane/ethyl acetate mixture (3/1 v/v) as the eluent, and precipitation in ether, 100 mg (yield: 17%) of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-6382314ae13e449e8e31eb63b6d50308
출처 메모uspto-grants-1993_09