HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 404714Erstellt: 25. Oktober 2026
4-Bromobenzaldehyde → N-(4-Bromobenzyl)-2,2-dimethoxyethanamine
https://huagongshe.com/reaction/404714
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Bromobenzaldehyde | HCID 70741 | — |
| Edukt | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Edukt | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-(4-Bromobenzyl)-2,2-dimethoxyethanamine | HCID 59226241 | 81,7% |
Reaktionsschritte
50 g (270.2 mmol) 4-bromobenzaldehyde were dissolved in 200 ml of toluene and 28.4 g (270.2 mmol) aminoacetaldehyde dimethylacetal were added. After the addition of 5.1 g (27.0 mmol) p-toluenesulfonic acid monohydrate, the reaction mixture was heated under reflux in a Dean Stark apparatus. After 4 h, the reaction was cooled to room temperature and washed with saturated sodium hydrogen carbonate-solution (2×) and water. The combined aqueous layers were extracted with Toluene and the combined organic layers were dried over magnesium sulfate and evaporated. The residue was dissolved in 200 ml of ethanol and 5.11 g (135.1 mmol) of sodium borohydride were added in small portions. After stirring for 2 h at room temperature and standing overnight, 5.0 ml acetic acid were added and the solvent was removed i. vac. The residue was taken up in dichloromethane and washed (2×) with water. After drying over magnesium sulfate and evaporation, 60.5 g of the title compound were obtained (crude product), which were used without further purification. Rt=0.80 min (Method C). Detected mass: 274.1/276.1 (M+H+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08748614B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-5d4402caa3d54c78a237de7453d9ab3a |
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| Quellennotiz | uspto-grants-2014_06 |
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