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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238268Generated: October 25, 2026

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

https://huagongshe.com/reaction/2238268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantCesium carbonateHCID 10796—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant5-(4-Hydroxybenzyl)thiazolidine-2,4-dioneHCID 10198397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-[4-(2,4-Dioxothiazolidin-5-ylmethyl)-phenoxy]-benzaldehydeHCID 5976829365.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718682B2
Source datasetuspto-grants-2010_05
ORD IDord-3f8585b470fd48e1bfaebd86db09f900
Source noteuspto-grants-2010_05