돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5994생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/5994

반응식

참여 물질

역할이름HCID투입량
반응물4-ThiobenzonitrileHCID 585058—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
촉매Zinc OxideHCID 3007857—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
생성물4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479533264%

반응 조건

온도50 °C

반응 단계

A suspension of 16.9 g (47.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 6 g (43.10-3 mol) of 4-mercaptobenzonitrile and 3.5 g (43.10-3 mol) of zinc oxide (ZnO) in 120 ml of anhydrous toluene and 120 ml of acetonitrile is stirred under an inert atmosphere, in the presence of a molecular sieve (1 mm), for 18 hours, at 50° C. After the reaction medium has been filtered on Celite® in ethyl acetate, the organic phase obtained is washed with a 1N solution of HCl twice, a 1N solution of sodium hydroxide and finally water, dried over magnesium sulfate and evaporated under reduced pressure. After precipitation in ether, 11.30 g (yield: 64%) of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-c325c2e4bd414d69a18ffb5e8f24076c
출처 메모uspto-grants-1993_09