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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854881Generated: October 26, 2026

Potassium Carbonate → ethyl 7-(4-methylbenzoyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTolylboronic acidHCID 79799—
Reactantethyl 7-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69517680—
CatalystHCID 178418476HCID 178418476—
Solvent1,4-DioxaneHCID 31275—
Productethyl 7-(4-methylbenzoyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 6951942441%

Reaction Conditions

Temperature80 °C

Reaction Steps

The ethyl 7-iodo-2-(trifluoromethyl)-2H-chromene-3-carboxylate from Example 9a, Step 2 (3.0 g, 7.53 mmol), 4-methylphenylboronic acid (1.11 g, 8.26 mmol), K2CO3 (3.12 g, 22.59 mmol), and PdCl2(PPh3)2 (159 mg, 0.225 mmol) were mixed in dioxane (30 mL) in a sterling bomb. Carbon monoxide was bubbling to 40 psi. The reaction was heated to 80° C. for 5 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 yellow solid (1.2 g, 41%): LCMS m/z 391.10 (M+H). 1H NMR (CDCl3/400 MHz) 7.75 (s, 1H), 7.69 (d, 2H, J=8.0 Hz), 7.39(d, 1H, J=8.0 Hz), 7.36 (s, 1H), 7.31 (d, 1H, J=8.0 Hz), 7.28 (d, 2H, J=8.0 Hz), 7.25(s, 1H), 5.78 (q, 1H, J=6 Hz), 4.33 (m, 2H), 2.43(s, 3H), 1.35 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-41b47c393ed0424b8ee4174a46d383a8
Source noteuspto-grants-2007_08