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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214834Generated: October 30, 2026

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

https://huagongshe.com/reaction/2214834

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

A mixture of 5-chlorosalicylaldehyde (20.02 g, 0.128 mole) and ethyl 4,4,4-trifluorocrotonate (23.68 g, 0.14 mole) was 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, 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, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109211B2
Source datasetuspto-grants-2006_09
ORD IDord-0016f68b62ae476d88b0f3ffaf42b011
Source noteuspto-grants-2006_09