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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855134Generated: October 28, 2026

Water → ethyl 7-(2,5-dimethylphenoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/855134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,5-DimethylphenolHCID 7267—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 58934808—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Productethyl 7-(2,5-dimethylphenoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69519100—

Reaction Conditions

Temperature110 °C

Reaction Steps

To 0.200 g (0.689 mmole) of ethyl 7-fluoro-2-(trifluoromethyl)-2H-chromene-3-carboxylate in 2.5 mL of DMF was added 0.118 g (0.946 mmol) of 2,5-dimethyl phenol to the vessel followed by 0.131 g (0.946 mmole) of potassium carbonate. The suspension was prepared in a capped vial and placed in a J-KEM heating block equipped with shaker, condenser and nitrogen atmosphere. The block was heated to 110° C. for 20hrs. For work up, 10 mL of H2O and 5 mL of ether was added to the mixture. The organic layer was separated and then the aqueous was extracted 3 times with ether. The product was then run through a pre-packed silica gel plug (20 mL, 5 g capacity) and the silica column washed with 4×5 mL aliquots of ether. Concentration of the solution afforded the product with was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-d1de590a92494864840d818b01c13910
Source noteuspto-grants-2007_08