돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 433209생성일: 2026년 10월 23일

Phosphate → 4-(Benzyloxy)butanoic acid

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

반응식

참여 물질

역할이름HCID투입량
반응물PhosphateHCID 1061—
반응물Sodium HydroxideHCID 14798—
반응물Sodium SulfateHCID 24436—
반응물4-Benzyloxy-1-butanolHCID 562212—
반응물Sodium HypochloriteHCID 23665760—
반응물Sodium ChloriteHCID 23668197—
촉매TempoHCID 2724126—
용매AcetonitrileHCID 6342—
생성물4-(Benzyloxy)butanoic acidHCID 562201102%

반응 조건

온도35 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06667325B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-bcb12d447c5142bfb0ae99809ba910cf
출처 메모uspto-grants-2003_12