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HRID 2217633作成日:2026年10月27日

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

https://huagongshe.com/reaction/2217633

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物Cesium carbonateHCID 10796—
反応物4-FluorobenzaldehydeHCID 68023—
反応物5-(4-Hydroxybenzyl)thiazolidine-2,4-dioneHCID 10198397—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物4-[4-(2,4-Dioxothiazolidin-5-ylmethyl)-phenoxy]-benzaldehydeHCID 5976829365.6%

反応条件

温度100 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07407978B2
出典データセットuspto-grants-2008_08
ORD IDord-72d878deb2b84d0185f350b9df887b87
出典メモuspto-grants-2008_08