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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854936Generated: October 30, 2026

Potassium Carbonate → ethyl 6-chloro-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-salicylaldehydeHCID 12481—
ReactantEthyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productethyl 6-chloro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 15458898138.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-Chlorosalicylaldehyde (20.02 g, 0.128 mole) and ethyl 4,4,4-trifluorocrotonate (23.68 g, 0.14 mole) were dissolved in anhydrous DMF, warmed to 60° C. and treated with anhydrous K2CO3 (17.75 g, 0.128 mole). The solution was maintained at 60° C. for 20 hours, cooled to room temperature, and diluted with water. The solution was extracted with ethyl acetate. The combined extracts were washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to afford 54.32 g of an oil. The oil was dissolved in 250 mL of methanol and 100 mL of water, whereupon a white solid formed that was isolated by filtration. The resulting solid was washed with water and dried in vacuo, to afford the ester as a yellow solid (24.31 g, 62%): mp 62-64° C. 1H NMR (CDCl3/90 MHz) 7.64 (s, 1H), 7.30-7.21 (m, 2H), 6.96 (d, 1H, J=Hz), 5.70 (q, 1H, J=Hz), 4.30 (q, 2H, J=7.2 Hz), 1.35 (t, 31H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-ccfd25e7525e459b9c382632a7136bd8
Source noteuspto-grants-2007_08