HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 885103Erstellt: 24. Oktober 2026
Hydrogen Peroxide → N-(4-bromo-2-fluorophenyl)-5,7-dimethylbenzo[d]oxazol-2-amine
https://huagongshe.com/de/reaction/885103
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | 6-Amino-2,4-xylenol | HCID 100530 | — |
| Edukt | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Edukt | 4-Bromo-2-fluorophenylisothiocyanate | HCID 2757003 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-(4-bromo-2-fluorophenyl)-5,7-dimethylbenzo[d]oxazol-2-amine | HCID 22347267 | — |
Reaktionsschritte
An ambient solution of 2-amino-4,6-dimethylphenol (0.85 g, 6.2 mmol) and 2-fluoro-4-bromophenyl isothiocyanate (1.44 g, 6.20 mmol) in tetrahydrofuran (20 mL) was stirred for 16 h. The reaction was cooled (0° C.), and LiOH.H2O (0.521 g, 12.41 mmol) was added, followed by the dropwise addition of 30% H2O2 (3.41 mL, 31.0 mmol) over 15 minutes. The reaction was warmed to room temperature and stirred for 16 h. The reaction was then quenched by the addition of 20% aqueous sodium sulfite solution (50 mL) and ethyl acetate (75 mL). The layers were separated, and the aqueous was extracted with additional ethyl acetate (2×75 mL). The combined organics were, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by chromatography on SiO2 gel, eluting with 25% ethyl acetate in hexane, to give the title compound. MS (ESI) m/z 335[M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08242139B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-ddde47f43ef44ce28af6c7bb74a78a96 |
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| Quellennotiz | uspto-grants-2012_08 |
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