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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 433209Erstellt: 24. Oktober 2026

Phosphate → 4-(Benzyloxy)butanoic acid

https://huagongshe.com/de/reaction/433209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphateHCID 1061—
EduktSodium HydroxideHCID 14798—
EduktSodium SulfateHCID 24436—
Edukt4-Benzyloxy-1-butanolHCID 562212—
EduktSodium HypochloriteHCID 23665760—
EduktSodium ChloriteHCID 23668197—
KatalysatorTempoHCID 2724126—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-(Benzyloxy)butanoic acidHCID 562201102%

Reaktionsbedingungen

Temperatur35 °C

Reaktionsschritte

3.0 g of 4-benyloxybutanol and 182 mg of TEMPO (2,2,6,6-tetramethyl-1-piperidinyloxy, radical) were dissolved in a mixture composed of 60 ml of acetonitrile and 60 ml of phosphate buffer (pH 6.7). To this reaction mixture were added 20 ml of an aqueous solution of sodium chlorite (NaClO2) (3.8 g) and 0.5 ml of a 5% aqueous solution of sodium hypochlorite (NaClO), followed by stirring at 35° C. for 5.5 hours. The reaction mixture was adjusted to pH 8.0 by the addition of a 2M aqueous solution of sodium hydroxide, and stirred for 20 minutes. Thereafter, 84 ml of an aqueous solution of sodium sulfate (5.1 g) was added thereto under cooling with ice so that its internal temperature would not exceed 20° C., followed by stirring for 30 minutes. After the reaction mixture was washed with 50 ml of t-butylmethyl ether, the aqueous solution was adjusted to pH 3-4 by the addition of 1M hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 3.3 g (102% yield) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06667325B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-bcb12d447c5142bfb0ae99809ba910cf
Quellennotizuspto-grants-2003_12