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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 530783Erstellt: 27. Oktober 2026

Ethyl Acetate → 4-(5-Chloro-2-methylbenzoxazol-6-yl)phenylamine

https://huagongshe.com/reaction/530783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt3-Aminophenylboronic acid hydrochlorideHCID 2763241—
Edukt6-Bromo-5-chloro-2-methylbenzoxazoleHCID 58487438—
KatalysatorBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelHexaneHCID 8058—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-(5-Chloro-2-methylbenzoxazol-6-yl)phenylamineHCID 6746729542%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A mixture of 6-bromo-5-chloro-2-methylbenzoxazole (54) (160 mg, 0.65 mmol), anilin-5-boronic acid hydrochloride salt (55) (135 mg, 1.2 eq), Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium (II) (A-Phos) (46 mg, 0.1 mmol) and K3PO4 (165 mg) in 2 ml ACN, 2 ml dioxane and 0.5 ml H2O was bubbled with argon before heated at 85° C. for 2 h. After cooling down to r.t., the reaction mixture was taken up in EA, washed with aq. NaHCO3 and brine, dried over Na2SO4, concentrated to dryness. The resulting red solid was dissolved in DCM and subjected to silica gel column purification using 0-60% B (A: hexane; B: 50% EA in hexane) to furnish 70.6 mg 56 as yellow solid (yield: 42%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09353099B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-a225d33d61544ebfb79172505de33767
Quellennotizuspto-grants-2016_05