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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2238268생성일: 2026년 10월 26일

Citric Acid → 4-[4-(2,4-Dioxothiazolidin-5-ylmethyl)-phenoxy]-benzaldehyde

https://huagongshe.com/reaction/2238268

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Cesium carbonateHCID 10796—
반응물4-FluorobenzaldehydeHCID 68023—
반응물5-(4-Hydroxybenzyl)thiazolidine-2,4-dioneHCID 10198397—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-[4-(2,4-Dioxothiazolidin-5-ylmethyl)-phenoxy]-benzaldehydeHCID 5976829365.6%

반응 조건

온도100 °C

반응 단계

To a solution of 52 (5.35 g, 24 mmol) in DMF (150 mL) was added 4-fluorobenzaldehyde (3.00 g, 24 mmol) and Cs2CO3 (20 g, 62 mmol) and the mixture was heated to 100° C. for 2 h. The mixture was poured over vigorously stirring 10% citric acid (200 mL) and ethyl acetate (200 mL). The organic layer was washed with water (300 mL), brine (300 mL), dried (MgSO4), filtered and concentrated in vacuo. The crude product was triturated in hexanes-ethyl acetate (2:1) to yield a white solid (5.15 g, 65%). 1H NMR: (400 MHz, DMSO-d6): δ 12.07 (bs, 1H), 9.92 (s, 1H), 7.92 (d, J=8.8 Hz, 2H), 7.35 (d, J=8.4 Hz, 2H), 7.12 (d, J=8.4 Hz, 2H), 7.09 (d, J=8.4 Hz, 2H) 4.94 (dd, J=8.4 and 4.4 Hz, 1H), 3.41 (dd, J=14.4 and 4.4 Hz, 1H), 3.17 (dd, J=14.4 and 9.2 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07718682B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-3f8585b470fd48e1bfaebd86db09f900
출처 메모uspto-grants-2010_05