HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 965130Erstellt: 24. Oktober 2026
Mercuric cyanide → N-[2-Methyl-5-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxymethyl)-phenyl]-3-nitrobenzamide
https://huagongshe.com/de/reaction/965130
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Mercuric cyanide | HCID 11591 | — |
| Edukt | Potassium Bromide | HCID 253877 | — |
| Edukt | N-(5-Hydroxymethyl-2-methylphenyl)-3-nitrobenzamide | HCID 19074226 | — |
| Edukt | alpha-D-glucopyranosyl bromide tetraacetate | HCID 86752853 | — |
| Katalysator | Mercury dibromide | HCID 24612 | — |
| Lösungsmittel | Nitromethane | HCID 6375 | — |
| Produkt | N-[2-Methyl-5-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxymethyl)-phenyl]-3-nitrobenzamide | HCID 67578982 | 57,2% |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05773420 |
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| Quelldatensatz | uspto-grants-1998_06 |
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| ORD ID | ord-233692c36e1f45f28397fc029598e4b7 |
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| Quellennotiz | uspto-grants-1998_06 |
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