HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1435063Erstellt: 26. Oktober 2026
Isoamylamine → (4-Bromo-2-chloro-benzyl)-(3-methyl-butyl)-amine
https://huagongshe.com/reaction/1435063
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Isoamylamine | HCID 7894 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 4-Bromo-2-chlorobenzaldehyde | HCID 14109109 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (4-Bromo-2-chloro-benzyl)-(3-methyl-butyl)-amine | HCID 57937814 | 95% |
Reaktionsschritte
4-bromo-2-chloro-benzaldehyde (I-3a: 10.0 g, 46.0 mmol) was dissolved in methanol and treated with isoamylamine (4.78 g, 54.7 mmol). After stirring overnight at room temperature, sodium borohydride (5.2 g, 138 mmol) was added to the reaction mixture. After stirring for 1 hour at room temperature, the reaction mixture was quenched using concentrated (37%) hydrochloric acid and the volatiles were removed under reduced pressure. The residue was taken up in an aqueous 2 N sodium hydroxide solution and extracted with ethyl acetate (2 times). The combined organic phases were washed with a saturated aqueous sodium bicarbonate solution, dried over sodium sulfate, filtered and concentrated under reduced pressure to afford the title product (I-3b: 12.7 g)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07615651B2 |
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| Quelldatensatz | uspto-grants-2009_11 |
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| ORD ID | ord-3091268a30c3421598847dc60ee415d1 |
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| Quellennotiz | uspto-grants-2009_11 |
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