HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2169182Erstellt: 25. Oktober 2026
Aluminium lithium hydride → Ethanol, 2-[(2,2,2-trifluoro-1-methylethyl)amino]-
https://huagongshe.com/reaction/2169182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Edukt | Oxazolidine, 2-methyl-2-(trifluoromethyl)- | HCID 43316684 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethanol, 2-[(2,2,2-trifluoro-1-methylethyl)amino]- | HCID 86725833 | 97,3% |
Reaktionsschritte
To a solution of 2-methyl-2-(trifluoromethyl)oxazolidine (39) (5.58 g, 36.0 mmol, Eq: 1.00) in tetrahydrofuran (30 ml) at 0° C. was added lithium aluminum hydride (2M solution in tetrahydrofuran) (18.0 ml, 36.0 mmol, Eq: 1.00) and the reaction mixture was stirred at room temperature for 1 hr, quenched slowly with 1 ml of cold water, stirred for 20 min. Then 1 ml of 1N NaOH aq. solution was added and the reaction mixture was stirred for 10 m in. 3 ml of water were added and the reaction mixture was stirred for 1 hr. Granular salt was formed. The white solid was filtered off, washed with diethyl ether (100 ml). The mixture was concentrated to obtain a crude product 2-(1,1,1-trifluoropropan-2-ylamino)ethanol (40) (oil, 5.50 g, 35.0 mmol, 97.3% yield) which was used as such in the next step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09045486B2 |
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| Quelldatensatz | uspto-grants-2015_06 |
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| ORD ID | ord-b936f9bb87574f629c7833ff56158075 |
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| Quellennotiz | uspto-grants-2015_06 |
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