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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 56613생성일: 2026년 10월 23일

2-Bromo-4'-nitroacetophenone → 3-[2-(4-Nitrophenyl)-2-oxoethyl]-1,3-thiazolidine-2,4-dione

https://huagongshe.com/ko/reaction/56613

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-4'-nitroacetophenoneHCID 66840—
반응물1,3-Thiazolidine-2,4-dione potassium saltHCID 87892318—
용매AcetoneHCID 180—
생성물3-[2-(4-Nitrophenyl)-2-oxoethyl]-1,3-thiazolidine-2,4-dioneHCID 11550894—

반응 조건

온도60 °C

반응 단계

A little at a time, 1.3 g (8.4 mmol) of 1,3-thiazolidine-2,4-dione potassium salt were added to a solution of 2.0 g (8.2 mmol) of 2-bromo-1-(4-nitrophenyl)ethanone in 80 ml of acetone, and the mixture was stirred at 60° C. for 1 h. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in water/dichloromethane. After phase separation, the organic phase was dried (sodium sulphate), filtered, concentrated under reduced pressure and dried. Yield: 2.3 g (98% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434690B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d1249409e06848c98d2c30682af412d3
출처 메모uspto-grants-2016_09