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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 556342Erstellt: 24. Oktober 2026

Benzyl Chloride → 6-Benzyloxy-benzo[d]isoxazole-3-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/556342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl ChlorideHCID 7503—
EduktCesium carbonateHCID 10796—
EduktEthyl 6-hydroxybenzo[d]isoxazole-3-carboxylateHCID 136216618—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Benzyloxy-benzo[d]isoxazole-3-carboxylic acid ethyl esterHCID 66992600—

Reaktionsbedingungen

Temperatur56 °C

Reaktionsschritte

To a solution of 0.98 g (4.73 mMol) 6-hydroxy-benzo[d]isoxazole-3-carboxylic acid ethyl ester [preparation see: J. Am. Chem. Soc. 97 (1974), 7305] in 100 ml acetone, 545 μl (4.73 mMol) benzylchloride, 3.08 g (9.46 mMol) Cs2CO3 und 10 mg NaI are added. Then the mixture is stirred for 2 h at rt and 5 h at 56° C. The reaction mixture is diluted with EtOAc and water, the aq. phase separated off and extracted with EtOAc. The organic layers are washed with water and brine, dried (Na2SO4) and concentrated after addition of 10 g SiO2. The resulting powder is put on top of a chromatography column (SiO2) and the title compound eluated with hexan/EtOAc 9:1→8:2→7:3: MS: [M+1]+=298; TLC(hexane/EtOAc 3:1): Rf=0.54.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08058276B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-d50dad6058f1460a8e5533089bfa5bdd
Quellennotizuspto-grants-2011_11