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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 479632Erstellt: 24. Oktober 2026

2,4,6-Tris((dimethylamino)methyl)phenol → Ethyl 7-(3-(2-propyl-4-phenoxyphenoxy)propoxy)-chromane-2-carboxylate

https://huagongshe.com/de/reaction/479632

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-Tris((dimethylamino)methyl)phenolHCID 7026—
EduktCesium carbonateHCID 10796—
EduktEthyl 7-hydroxychromane-2-carboxylateHCID 11085381—
Edukt1-(3-bromopropoxy)-4-phenoxy-2-propylBenzeneHCID 18772273—
ProduktEthyl 7-(3-(2-propyl-4-phenoxyphenoxy)propoxy)-chromane-2-carboxylateHCID 1877226676%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a 50 ml round-bottom flask were added ethyl 7-hydroxychromane-2-carboxylate (100 mg, 0.45 mmol), 4-(3-bromopropoxy)-3-propylphenyl phenyl ether (U.S. Pat. No. 6,008,237) (188 mg, 0.54 mmol), cesium carbonate (176 mg, 0.54 mmol), and DMF 3 ml. The resulting suspension was stirred at 70° C. for 5 hr. The solvent was removed under reduced pressure. The residue was diluted with AcOEt and water. The organic layer was separated. The aqueous layer was extracted twice with AcOEt. The combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated, and chromatographed on silica gel. Eluting with 10% AcOEt/hexanes gave the title compound as a pale yellow oil 167 mg (76%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06645997B2
Quelldatensatzuspto-grants-2003_11
ORD IDord-de6e3a706af54bc49ab9fde730dd9b1b
Quellennotizuspto-grants-2003_11