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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854886Generated: October 26, 2026

Potassium Carbonate → ethyl 7-(2-furyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantFuran-2-boronic acidHCID 2734357—
Reactantethyl 7-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69517680—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Productethyl 7-(2-furyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 6951840921%

Reaction Conditions

Temperature80 °C

Reaction Steps

The ethyl 7-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylate from Example 9a, Step 2 (2.0 g, 5.02 mmol), 2-furylboronic acid (0.62 g, 5.52 mmol), K2CO3 (2.08 g, 15.06 mmol), and PdCl2(PPh3)2 (106 mg, 0.15 mmol) were mixed in dioxane (20 mL) in a sterling bomb. Carbon monoxide was bubbling to 40 psi. The reaction was heated to 80° C. for 12 h. After filtration, the reaction was quenched with NH4Cl and extracted with EtOAc. The organic layer was washed and dried over MgSO4. The filtrate was evaporated and dried in vacuo to afford crude which was purified Biotage Chromatography with 10 to 20% ethyl acetate in hexane to give yellow solid (350 mg, 21%): LCMS m/z 339.05 (M+H). 1H NMR (CDCl3/300 MHz) 7.74 (s, 1H), 7.51 (s, 1H), 8.97 (m, 3H), 6.76 (d, 1H, J=3.3 Hz), 6.51 (m, 1H), 5.73 (q, 1H, J=6.9 Hz), 4.34 (m,2H), 1.36 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-5bc26005c1b4475992ea3105f6e94e4f
Source noteuspto-grants-2007_08