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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507261Erstellt: 23. Oktober 2026

Ethyl bromoacetate → ethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetate

https://huagongshe.com/de/reaction/507261

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktPotassium CarbonateHCID 11430—
Edukt2-MercaptobenzimidazoleHCID 707035—
LösungsmittelEthanolHCID 702—
Produktethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetateHCID 2156430.947,1%

Reaktionsschritte

To a stirred solution of 1H-benzo[d]imidazole-2(3H)-thione (20.0 g, 0.13 mol, 1.0 eq.) in anhydrous ethanol (500 mL) at room temperature, was added potassium carbonate (9.25 g, 0.07 mol, 0.5 eq.) and ethyl bromoacetate (26.7 g, 0.16 mmol, 1.2 eq.). The reaction was heated to reflux and stirred at that temperature for 6 hours. The solvent was removed in vacuo and water (200 mL) was added. The aqueous phase was extracted with dichloromethane (3×100 mL), and the combined organic extracts were washed with water (200 mL) and brine (200 mL). The organic phase was dried over magnesium sulfate and concentrated in vacuo to give a colorless oil which solidified on standing. Purification by flash chromatography (CHCl3→10% MeOH:90% CHCl3) gave 4a as a white solid (11.7 g, 37%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07786139B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-5334d5798f48437cbdff6f8e3432540f
Quellennotizuspto-grants-2010_08