돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248694생성일: 2026년 10월 24일

Hydrochloric Acid → Benzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-

https://huagongshe.com/ko/reaction/248694

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물3-Aminobenzoic AcidHCID 7419—
반응물TriethylamineHCID 8471—
반응물2-Acetylthiomethyl-3-phenyl-propionyl chlorideHCID 10377734—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물Benzoic acid, 3-[[2-[(acetylthio)methyl]-1-oxo-3-phenylpropyl]amino]-HCID 1021555241.3%

반응 단계

3-Aminobenzoic acid (1.4 g) is suspended in chloroform (50 ml), and thereto is added triethylamine (2.06 g), and to the mixture is added 2-acetylthiomethyl-3-phenylpropionyl chloride (2.61 g) with stirring under ice cooling, and the mixture is stirred for 30 minutes and further at room temperature three nights. To the reaction mixture is added water, and the mixture is acidified with hydrochloric acid and extracted with chloroform. The extract is washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue is purified by a medium pressure column chromatography with CHP-20P (eluant, water-acetonitrile). The fractions containing the desired compound are collected and concentrated under reduced pressure. The precipitates are separated by filtration and recrystallized from 50% aqueous ethanol to give the title compound (1.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05210266
출처 데이터셋uspto-grants-1993_05
ORD IDord-9086da73e5914ea48feda8ed24d0bab9
출처 메모uspto-grants-1993_05