돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1422298생성일: 2026년 10월 27일

(R)-2-Bromo-3-phenylpropionic acid → (S)-2-acetylthio-3-phenylpropanoic acid

https://huagongshe.com/reaction/1422298

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2-Bromo-3-phenylpropionic acidHCID 11746403—
반응물Potassium ethanethioateHCID 23670855—
촉매Trioctylmethylammonium chlorideHCID 21218—
용매Ethyl AcetateHCID 8857—
생성물(S)-2-acetylthio-3-phenylpropanoic acidHCID 10176891—

반응 단계

In a 3 l-jacketed reactor, with mechanical stirring, refrigerator and thermometer, (R)-2-bromo-3-phenyl-propionic acid (385.8 g, 1.68 moles), ethyl acetate (1,143 ml) and ALIQUAT 336° (4.2 g, 0.01 mole) were charged at 15° C. under nitrogen flow. The mixture temperature was brought to 0° C. and potassium thioacetate (222 g, 1.944 moles) was added in two portions. The reaction temperature was kept at 15° C. for 6 hours, then the mixture was twice washed with an aqueous solution of sodium thiosulfate pentahydrate (84.6 g in 820 ml of water over-all), then twice with demineralized water (600 ml total). The phases were separated and the organic one was concentrated under vacuum in a thermostated bath at 35-40° C. The resulting organic solution was cooled and filtered over celite, then added with ethyl acetate (600 ml). On the basis of the HPLC analysis, the yield in solution was equal to 87%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06080881
출처 데이터셋uspto-grants-2000_06
ORD IDord-978049f1b20247c99f74fde8785d163b
출처 메모uspto-grants-2000_06