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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5993생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/5993

반응식

참여 물질

역할이름HCID투입량
반응물4-ThiobenzonitrileHCID 585058—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranosyl trichloroacetimidateHCID 21631547—
촉매ZincchlorideHCID 3007855—
용매AcetonitrileHCID 6342—
생성물4-cyanophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1479533223%

반응 단계

A suspension of 192 mg (0.44.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl trichloroacetimidate, 71 mg (0.52.10-3 mol) of 4-mercaptobenzonitrile, 20 mg (0.15.10-3 mol) of zinc chloride and a 400 pm sieve in 2 ml of acetonitrile is stirred for 4 h under an inert atmosphere. The reaction mixture is then filtered on Celite® in ethyl acetate and subsequently washed with 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 precipitation in ether, 42 mg (yield: 23%) of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-783281c6407248d1a55de54558cee7a5
출처 메모uspto-grants-1993_09