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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 965130생성일: 2026년 10월 25일

Mercuric cyanide → N-[2-Methyl-5-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxymethyl)-phenyl]-3-nitrobenzamide

https://huagongshe.com/reaction/965130

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참여 물질

역할이름HCID투입량
반응물Mercuric cyanideHCID 11591—
반응물Potassium BromideHCID 253877—
반응물N-(5-Hydroxymethyl-2-methylphenyl)-3-nitrobenzamideHCID 19074226—
반응물alpha-D-glucopyranosyl bromide tetraacetateHCID 86752853—
촉매Mercury dibromideHCID 24612—
용매NitromethaneHCID 6375—
생성물N-[2-Methyl-5-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxymethyl)-phenyl]-3-nitrobenzamideHCID 6757898257.2%

반응 단계

A mixture of N-(5-hydroxymethyl-2-methylphenyl)-3-nitrobenzamide (10.0 g, 0.034 mol), HgBr2 (10.0 g, 0.041 mol), Hg(CN)2 (15.0 g, 0.058 mol), and α-D-glucopyranosyl bromide tetraacetate (17.2 g, 0.042 mol) in nitromethane (200 mL) was heated under reflux for 4 h. 2.0M KBr was added and the mixture was stirred for 30 minutes and extracted with EtOAc. The combined extracts were washed with saturated aqueous NaHCO3 and brine, dried (MgSO4), and concentrated to give 12.0 g (56%) of product as a brown foam; 1H NMR (DMSO-d6) δ2.00 (m, 12 H), 2.21 (s, 3 H), 4.00 (m, 2 H), 4.20 (dd, J=12.4, 5.0 Hz, 1 H), 4.58 (d, J=12.4 Hz, 1 H), 4.82 (m, 4 H), 5.27 (t, J=9.3 Hz, 1 H), 7.10 (d, J=7.8 Hz, 1 H), 7.24 (d, J=7.8 Hz, 1 H), 7.25 (s, 1 H), 7.81 (m, 1 H), 8.42 (m, 2 H), 8.80 (s, 1 H), 10.60 (s, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773420
출처 데이터셋uspto-grants-1998_06
ORD IDord-233692c36e1f45f28397fc029598e4b7
출처 메모uspto-grants-1998_06