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HRID 965130作成日:2026年10月26日

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

https://huagongshe.com/reaction/965130

反応式

関与物質

役割名称HCID仕込み量
反応物Mercuric cyanideHCID 11591—
反応物Potassium BromideHCID 253877—
反応物N-(5-Hydroxymethyl-2-methylphenyl)-3-nitrobenzamideHCID 19074226—
反応物alpha-D-glucopyranosyl bromide tetraacetateHCID 86752853—
触媒Mercury dibromideHCID 24612—
溶媒NitromethaneHCID 6375—
生成物N-[2-Methyl-5-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxymethyl)-phenyl]-3-nitrobenzamideHCID 6757898257.2%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05773420
出典データセットuspto-grants-1998_06
ORD IDord-233692c36e1f45f28397fc029598e4b7
出典メモuspto-grants-1998_06