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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 885104Erstellt: 25. Oktober 2026

Hydrogen Peroxide → N-(4-bromophenyl)-7-methylbenzo[d]oxazol-2-amine

https://huagongshe.com/reaction/885104

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
Edukt4-Bromophenyl isothiocyanateHCID 16133—
EduktLithium hydroxide, monohydrateHCID 168937—
Edukt6-Amino-o-cresolHCID 413657—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(4-bromophenyl)-7-methylbenzo[d]oxazol-2-amineHCID 68721392—

Reaktionsschritte

An ambient solution of 2-amino-6-methylphenol (0.74 g, 6.0 mmol) and 4-bromophenyl isothiocyanate (1.28 g, 6.0 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 303[M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08242139B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-61d75497f0f546a1bf1372e3cd63836b
Quellennotizuspto-grants-2012_08