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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4394생성일: 2026년 10월 23일

Acetic Acid → 5-{4-[2-(5-Methyl-2-phenyl-4-oxazolyl)-2-oxoethoxy]benzylidene}-2,4-thiazolidinedione

https://huagongshe.com/ko/reaction/4394

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium hydrideHCID 24758—
반응물5-((4-Hydroxyphenyl)methylene)-2,4-thiazolidinedioneHCID 517822—
반응물2-Bromo-1-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethan-1-oneHCID 14913650—
용매DimethylformamideHCID 6228—
생성물5-{4-[2-(5-Methyl-2-phenyl-4-oxazolyl)-2-oxoethoxy]benzylidene}-2,4-thiazolidinedioneHCID 5390813333.3%

반응 단계

60% sodium hydride in oil (0.24 g) was added to a solution of 5-(4-hydroxybenzylidene)-2,4-thiazolidinedione (0.663 g) in N,N-dimethylformamide (20 ml) and the mixture was stirred for 30 minutes. Then, a solution of 4-bromoacetyl-5-methyl-2-phenyloxazole (0.841 g) in N,N-dimethylformamide (10 ml) was added dropwise to the mixture under ice-cooling. After stirring under ice-cooling for 30 minutes, the reaction solution was poured into ice-cold water. The aqueous mixture was made acid with acetic acid. The solid which precipitated was collected by filtration, washed with water, and crystallized from acetone to give 5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)-2-oxoethoxy]benzylidene}-2,4-thiazolidinedione (0.42 g, 32.3%). Recrystallization from chloroform-ethanol yielded colorless needles, m.p. 244°-245° C. Elemental analysis for C22H16N2O5S, Calcd.: C, 62.85; H, 3.84; N, 6.66. Found: C, 62.80; H, 3.69; N, 6.93.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725610
출처 데이터셋uspto-grants-1988_02
ORD IDord-b11cbb3989ca4572a78c632b845a4b6a
출처 메모uspto-grants-1988_02