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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7800Generated: October 25, 2026

Phosphate → 4-(Benzyloxy)butanoic acid

https://huagongshe.com/reaction/7800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactant4-Benzyloxy-1-butanolHCID 562212—
ReactantSodium HypochloriteHCID 23665760—
ReactantSodium ChloriteHCID 23668197—
CatalystTempoHCID 2724126—
SolventAcetonitrileHCID 6342—
Product4-(Benzyloxy)butanoic acidHCID 562201102%

Reaction Conditions

Temperature35 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087624B2
Source datasetuspto-grants-2006_08
ORD IDord-b804c6c0279240b3a7262672a29b0e17
Source noteuspto-grants-2006_08