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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2059958Erstellt: 26. Oktober 2026

Diethyl Ether → ethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetate

https://huagongshe.com/reaction/2059958

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktBenzyl BromideHCID 7498—
Eduktethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetateHCID 21564—
EduktSodium hydrideHCID 24758—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetateHCID 97543131%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred solution of ethyl 2-(1H-benzo[d]imidazol-2-ylthio)acetate 4a (11.2 g, 47.6 mmol, 1.0 eq.) in 10:1 diethyl ether:dimethylformamide (450 mL) at 0° C., was added 60% sodium hydride in mineral oil (2.09 g, 52.3 mmol, 1.1 eq.), and the reaction was stirred at 0° C. for 20 minutes. Benzyl bromide (9.78 g, 57.1 mmol, 1.2 eq.) was added at 0° C., and the reaction was stirred with warming to room temperature for 16 hours. The reaction mixture was quenched with methanol (100 mL) and concentrated in vacuo. The residue was taken into hot chloroform (400 mL) and filtered. The filtrate was washed with water (200 mL), 1M HCl (200 mL) and brine (200 mL). The organic layer was dried over magnesium sulfate and concentrated in vacuo. Purification by flash chromatography (10% EtOAc:90% petroleum ether) gave 4b as a pale-yellow solid (4.82 g, 30%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08278327B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-78ec53df199c44c4b210f4fb9b37d8e2
Quellennotizuspto-grants-2012_10