HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 855206Erstellt: 24. Oktober 2026
2-Amino-1-(4-fluorophenyl)ethan-1-ol → [Rac]-(4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amine
https://huagongshe.com/de/reaction/855206
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Amino-1-(4-fluorophenyl)ethan-1-ol | HCID 9827 | — |
| Edukt | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water ethylacetate | HCID 22728543 | — |
| Produkt | [Rac]-(4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amine | HCID 69342608 | — |
Reaktionsschritte
0.52 ml of 4-tert-butylbenzaldehyde (3.1 mmol) and 320 mg of [rac]-2-amino-1-(4-fluoro-phenyl)-ethanol (2.06 mmol) were dissolved in 15 ml methanol at rt, and after stirring for 5 min at rt, were refluxed for 2 h. After cooling down to rt, 117 mg (3.1 mmol) of sodium borohydride were added and after stirring for 15 min at rt, the reaction mixture was then refluxed for 2 h. After cooling down to rt, the residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was stirred with diethylether/heptane, filtered and the solid dried under high vacuo, leading to 410 mg of [rac]-(4-tert-butyl-benzyl)-[2-(4-fluoro-phenyl)-2-hydroxy-ethyl]-amine as a white solid (66%). MS (ISP) 302.2 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07259183B2 |
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| Quelldatensatz | uspto-grants-2007_08 |
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| ORD ID | ord-1a908dc1f5b248aeac627f21184b3903 |
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| Quellennotiz | uspto-grants-2007_08 |
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