HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77896Erstellt: 23. Oktober 2026
Dimethylformamide → 2-(4-Bromo-benzyloxy)4-methyl-pyridine
https://huagongshe.com/de/reaction/77896
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Edukt | 2-Fluoro-4-methylpyridine | HCID 2737403 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-(4-Bromo-benzyloxy)4-methyl-pyridine | HCID 59255288 | 58,8% |
Reaktionsschritte
To a mixture of 4-bromobenzyl alcohol (4.54 g, 24.3 mmol) and N,N-dimethylformamide (50.0 mL) were added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) was added at 0° C. under nitrogen atmosphere, which was stirred for 50 minutes at room temperature. 2-Fluoro-4-methylpyridine (1.80 g, 16.2 mmol) was then added thereto at 0° C., and stirred for 2 hours and 30 minutes at room temperature. Water was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was separated, washed with saturated aqueous sodium chloride, and filtered. The filtrate was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:15) to obtain the title compound (2.65 g, 58.8%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841327B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-79efb6ff36ff47b189d35a939edd6e29 |
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| Quellennotiz | uspto-grants-2014_09 |
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