HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507262Erstellt: 24. Oktober 2026
Diethyl Ether → ethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetate
https://huagongshe.com/de/reaction/507262
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | ethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetate | HCID 21564 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | ethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetate | HCID 975431 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07786139B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-39bea83ebfac46b2b16214d7f5e1304e |
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| Quellennotiz | uspto-grants-2010_08 |
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