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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1457326생성일: 2026년 10월 26일

2-Benzoylbenzoic Acid → 3-(2-Benzoylbenzoyl)-4-thiazolidinemethanol

https://huagongshe.com/reaction/1457326

반응식

참여 물질

역할이름HCID투입량
반응물2-Benzoylbenzoic AcidHCID 6813—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물4-ThiazolidinemethanolHCID 321333—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
용매DichloromethaneHCID 6344—
생성물3-(2-Benzoylbenzoyl)-4-thiazolidinemethanolHCID 2210446640%

반응 단계

1.9 g (8.4 mmol) of o-benzoylbenzoic acid and 1.13 g (8.4 mmol) of 1-hydroxybenzotriazole hydrate were combined in 50 ml of methylene chloride and stirred for 20 minutes at room temperature. 1.0 g (8.4 mmol) of 4-thiazolidinemethanol was added, followed by 1.6 g (8.4 mmol) of ethyl-3-(3-dimethylaminopropyl)carbodiimide. The reaction mixture was stirred for 18 hours at room temperature and washed with water, first at pH 2.5 and then at pH 9.5. The organic phase was dried and evaporated to give a foam which was chromatographed on silica gel using 1:1/chloroform:ethyl acetate as the eluant to yield 1.1 g (40%) of the title compound. 1H NMR (CDCl3) δ: 7.4-7.85(m,9H); 4.65(m,1H) ; 4.20-4.40(m,2H); 3.96(m,1H); 3.60-3.70(m,2H); 3.0-3.30(m,2H). High Resolution Mass Spectrum: m/e=328.1015±0.8 ppm (calculated for C18H18NO3S).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05847155
출처 데이터셋uspto-grants-1998_12
ORD IDord-21cea4eb360c472eb84462b7a0d7079c
출처 메모uspto-grants-1998_12