HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2403333Erstellt: 24. Oktober 2026
Hydroxyamine hydrochloride → (R)-tert-butyl 2-(4-amino-2-fluorophenyl)morpholine-4-carboxylate
https://huagongshe.com/de/reaction/2403333
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | (R)-tert-butyl 2-(4-(diphenylmethyleneamino)-2-fluorophenyl)morpholine-4-carboxylate | HCID 86671413 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (R)-tert-butyl 2-(4-amino-2-fluorophenyl)morpholine-4-carboxylate | HCID 68325616 | 85% |
Reaktionsschritte
To a stirred solution of (R)-tert-butyl 2-(4-(diphenylmethyleneamino)-2-fluorophenyl)morpholine-4-carboxylate (5.95 g) in methanol (50 ml) were added sodium acetate (2.93 g) and hydroxylamine hydrochloride (1.82 g). The reaction mixture was stirred at 50° C. overnight. The reaction mixture was then filtered through sintered glass and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (silica gel; gradient: 0% to 60% EtOAc in hexanes) to afford (R)-tert-butyl 2-(4-amino-2-fluorophenyl)morpholine-4-carboxylate (3.0 g, 85%) as a yellow solid. MS (ISP): 296 ([M]+), 240 ([M-C4H8]+), 195 ([M+H—C4H8—CO2H]+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08802673B2 |
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| Quelldatensatz | uspto-grants-2014_08 |
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| ORD ID | ord-01db3347afd7432ca5c5909882a549b5 |
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| Quellennotiz | uspto-grants-2014_08 |
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