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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324177Erstellt: 25. Oktober 2026

Ethyl Acetate → HCID 22003490, Verbindung

https://huagongshe.com/reaction/324177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktTrimethyl orthobeznoateHCID 69720—
EduktSodium BicarbonateHCID 516892—
EduktHCID 22003462HCID 22003462—
Katalysatorp-Toluenesulfonic acid monohydrateHCID 521998—
LösungsmittelWaterHCID 962—
ProduktHCID 22003490HCID 2200349078,4%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

To 1.00 mL (5.82 mmol) of trimethyl orthobenzoate was added 204 mg (0.70 mmol) of 5-(4-amino-3-hydroxy-5-methoxyphenyl)-4-t-butyl-3,3-dimethyl-2,3-dihydrofuran (Compound [61]), and the mixture was refluxed for 1.5 hours at 150° C. To this reaction mixture, 2.0 ml of ethyl acetate, and 0.2 ml of H2O, and 10.1 mg (0.05 mmol) of TsOH H2O was added and the mixture was refluxed for 1 hours at 97° C. The resulting mixture was poured in saturated aqueous solution of sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride, dried with magnesium sulfate anhydride, and concentrated. The residue was applied to a silica gel column and the elution was carried out with the mixture of hexane and ethyl acetate (hexane:ethyl acetate=10:1) to obtain 207 mg of 4-t-butyl-5-(4-methoxy-2-phenylbenzo[d]oxazol-6-yl)-3,3-dimethyl-2,3-dihydrofuran (Compound [62]). Yield 78.4%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218135B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-e28e0a4c74f4496e94cd8757a337ce1d
Quellennotizuspto-grants-2001_04