HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 522849Erstellt: 25. Oktober 2026
Acetic Acid → N-(4-Bromobenzyl)-2,2-dimethoxyethanamine
https://huagongshe.com/reaction/522849
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 4-Bromobenzaldehyde | HCID 70741 | — |
| Edukt | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-(4-Bromobenzyl)-2,2-dimethoxyethanamine | HCID 59226241 | 73% |
Reaktionsschritte
To an ice-cold solution of 4-bromo-benzaldehyde (10 g, 0.05 mol) and 2,2-dimethoxy-ethylamine (6.8 g, 0.06 mol) in MeOH (200 mL) was added AcOH (2 mL), and the reaction mixture was stirred at RT for 1 h. The reaction mixture was cooled to 0° C. and NaBH4 (6.2 g, 0.15 mol) was added portionwise. The reaction mixture was stirred at RT for 10 h. After completion, The resulting reaction mixture was concentrated under reduced pressure and 10% aqueous NaOH was added. The mixture was extracted with EtOAc, the organic layer separated, dried over Na2SO4, and concentrated under reduced pressure. Purification was done by column chromatography using 100-200 mesh silica gel eluting with 5-15% EtOAc in hexanes to afford N-(4-bromobenzyl)-2,2-dimethoxyethanamine (10 g, 67%) as a pale yellow liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09334269B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-be8d3061f31b411a919d5233dcde361e |
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| Quellennotiz | uspto-grants-2016_05 |
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