HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484115Erstellt: 23. Oktober 2026
Dimethylformamide → N,N-dimethyl-3-[4-(trifluoromethyl)phenoxy]benzenepropanamine
https://huagongshe.com/de/reaction/484115
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Benzene, 1-fluoro-4-(trifluoromethyl)- | HCID 67873 | — |
| Edukt | 3-(Dimethylamino)-1-phenylpropan-1-ol | HCID 110665 | — |
| Produkt | N,N-dimethyl-3-[4-(trifluoromethyl)phenoxy]benzenepropanamine | HCID 19736879 | 100% |
Reaktionsschritte
Sodium borohydride (6.7 g) was slowly added to a solution of 3-dimethylaminopropiophenone (15.5 g) in 2-propanol (125 ml) and methanol (25 ml). After two hrs, the reaction mixture was stirred with water and extracted with ethyl acetate-ether. The organic extract was washed with water and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated to give 15.2 g (97%) of 3-dimethylamino-1-phenyl-1-propanol, as an oil. A solution of 3-dimethylamino-1-phenyl-1-propanol (15 g) in dimethylformamide (75 ml) was slowly added to a suspension of sodium hydride (60% oil-dispersion, washed with hexane, 5.5 g) in dimethylformamide (20 ml). A solution of 4-fluorobenzotrifluoride (18 g) in dimethylformamide (20 ml) was added. After two hrs, the reaction mixture was stirred with ice-water and extracted with ether. The ether extract was dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated to provide 27 g (100%) of N,N-dimethyl-3-[ 4-(trifluoromethyl)phenoxy]benzenepropanamine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05229417 |
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| Quelldatensatz | uspto-grants-1993_07 |
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| ORD ID | ord-d60792aba5b04511864f800cc25d0407 |
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| Quellennotiz | uspto-grants-1993_07 |
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