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HRID 433209作成日:2026年10月24日

Phosphate → 4-(Benzyloxy)butanoic acid

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

反応式

関与物質

役割名称HCID仕込み量
反応物PhosphateHCID 1061—
反応物Sodium HydroxideHCID 14798—
反応物Sodium SulfateHCID 24436—
反応物4-Benzyloxy-1-butanolHCID 562212—
反応物Sodium HypochloriteHCID 23665760—
反応物Sodium ChloriteHCID 23668197—
触媒TempoHCID 2724126—
溶媒AcetonitrileHCID 6342—
生成物4-(Benzyloxy)butanoic acidHCID 562201102%

反応条件

温度35 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06667325B1
出典データセットuspto-grants-2003_12
ORD IDord-bcb12d447c5142bfb0ae99809ba910cf
出典メモuspto-grants-2003_12