HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2043349Erstellt: 24. Oktober 2026
Acetic Acid → (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine
https://huagongshe.com/de/reaction/2043349
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 3-Benzyloxyaniline | HCID 92892 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 6-Bromopyridine-2-carbaldehyde | HCID 2757009 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine | HCID 86620293 | 80% |
Reaktionsschritte
To a solution of 3-benzyloxyaniline (0.70 g, 3.51 mmol) in 1,2-dichloroethane (10 ml) were added 6-bromo-pyridine-2-carboxaldehyde (0.65 g, 3.51 mmol), sodium triacetoxyborohydride (1.49 g, 7.03 mmol) and acetic acid (0.80 ml, 14.1 mmol). The reaction mixture was shaken at 40° C. overnight. For work-up dichloromethane (100 ml) and 1 M sodium bicarbonate solution (40 ml) were added and the mixture was shaken. The organic layer was separated, dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (heptane/ethyl acetate=3:1) to yield an orange oil (1.03 g, 80%); MS (ISP): 371.1 ([81Br M+H]+), 369.1 ([79Br M+H]+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08586617B2 |
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| Quelldatensatz | uspto-grants-2013_11 |
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| ORD ID | ord-d8f9716ec6ae47d4b562a9d806cb07a0 |
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| Quellennotiz | uspto-grants-2013_11 |
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