HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2394314Erstellt: 25. Oktober 2026
Ammonium Acetate → 2-(4-Chlorophenoxy)-1-methylpropylamine
https://huagongshe.com/reaction/2394314
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Acetate | HCID 517165 | — |
| Edukt | 3-(4-Chlorophenoxy)-2-butanone | HCID 3722632 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2-(4-Chlorophenoxy)-1-methylpropylamine | HCID 18972724 | 86% |
Reaktionsschritte
82 g of ammonium acetate and 6.7 g of sodium cyanoborohydride were added to a solution containing 21 g of 3-(4-chlorophenoxy)-2-butanone dissolved in 500 ml of methanol, and the reaction mixture was stirred for 20 hours at room temperature. After the reaction mixture was concentrated under reduced pressure, 180 ml of concentrated hydrochloric acid, 100 ml of water, and 300 ml of diethyl ether were added to the residue. The obtained water layer was alkalified using a 5% aqueous solution of sodium hydroxide, and then the organic substances were extracted with 500 ml of ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. A fraction possessing a low boiling point was removed from the obtained oily products to afford 18 g (yield 86%) of the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05811424 |
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| Quelldatensatz | uspto-grants-1998_09 |
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| ORD ID | ord-7bca85b58ba14edd93d1a42b3fda365b |
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| Quellennotiz | uspto-grants-1998_09 |
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