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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55080Erstellt: 23. Oktober 2026

4-Nitrobenzenethiol → 2-[(4-Nitrophenyl)sulfanyl]-1H-benzimidazole

https://huagongshe.com/de/reaction/55080

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzenethiolHCID 15809—
Edukt2-ChlorobenzimidazoleHCID 78572—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
LösungsmittelEthanolHCID 702—
Produkt2-[(4-Nitrophenyl)sulfanyl]-1H-benzimidazoleHCID 1261762515,3%

Reaktionsschritte

2-Chlorobenzimidazole (0.033 moles, 5.0 g), 4-nitrothiophenol (0.033 moles, 4.14 g), and DBU (0.033 moles, 5.0 g) in 200 ml ethanol were heated at 55° C. for 3 hr. The reaction was concentrated, ethyl acetate added, washed with water, dried over sodium sulfate and the solvent removed. The solid was slurred in hexane to yield 2-(4-nitrophenylthio)benzimidazole 1.37 g, 15%. Mass Spec (FD) 271. Calculated for C13H8N3O2S: C, 57.55; H, 3.34; N, 15.49. Found: C, 57.50; H, 5.54; N, 15.23.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624937
Quelldatensatzuspto-grants-1997_04
ORD IDord-e19f3c68bd474193823c5cefc616e6b8
Quellennotizuspto-grants-1997_04