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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5996생성일: 2026년 10월 24일

Mercuric cyanide → 4-nitrophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranoside

https://huagongshe.com/ko/reaction/5996

반응식

참여 물질

역할이름HCID투입량
반응물Mercuric cyanideHCID 11591—
반응물4-NitrobenzenethiolHCID 15809—
반응물2,3,4-tri-O-acetyl-5-thio-alpha-xylopyranosyl bromideHCID 10926314—
생성물4-nitrophenyl 2,3,4-tri-O-acetyl-1,5-dithio-beta-D-xylopyranosideHCID 1064624066%

반응 단계

If the procedure described in Preparation I is followed starting from 6 g (38.10-3 mol) of 4-nitrobenzenethiol, 10.7 g (42.10-3 mol) of mercuric cyanide, Hg(CN)2, and 15.1 g (42.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl bromide, 10.8 g (yield: 66%) of the expected product are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246961
출처 데이터셋uspto-grants-1993_09
ORD IDord-6e155a0fcdfe4261a9d6e2ec6bcd8028
출처 메모uspto-grants-1993_09