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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511946Generated: October 26, 2026

Potassium Carbonate → Ethyl acetate hexane

https://huagongshe.com/reaction/511946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactant(5-Bromonaphthalen-1-yl)methanolHCID 18963829—
Reactant(2-Methoxy-4-(trifluoromethyl)phenyl)boronic acidHCID 24901776—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl acetate hexaneHCID 2122620686%

Reaction Conditions

Temperature100 °C

Reaction Steps

(5-Bromonaphthalen-1-yl)methanol (150 mg), 2-methoxy-4-trifluoromethylphenylboronic acid (167 mg, 1.2 eq.), Pd(OAc)2 (14 mg, 0.1 eq.), Xphos (60 mg, 0.2 eq.), and K2CO3 (262 mg, 3 eq.) were combined in a flask with 5 mL dioxane and 1.6 mL H2O and degassed. Reaction mixture was then refluxed at 100° C. for 2 hours. Solution was cooled to room temperature then diluted with EtOAc and washed with saturated NaHCO3. The organic layer was dried over sodium sulfate and concentrated. Chromatography achieved using ISCO max gradient 35% EtOAc/hexane yielding product as a clear oil (55 mg, 86% yield). 1H NMR (400 MHz) (CDCl3) δ 8.24-8.22 (m, 1H), 7.64 (dd, J=8 Hz, J=8 Hz, 1H), 7.55 (d, J=8 Hz, 1H), 7.51 (d, J=8 Hz, 1H), 7.45-7.37 (m, 4H), 7.29 (s, 1H), 5.22 (s, 2H), 3.76 (s, 3H). 13C NMR (100 MHz) (CDCl3) δ157.45, 136.48, 136.27, 133.49, 132.21, 132.16, 131.47, 131.29, 131.15, 127.29, 126.61, 125.77, 125.48, 125.41, 123.88, 122.79, 117.44, 117.40, 107.72, 63.94, 55.76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102617B2
Source datasetuspto-grants-2015_08
ORD IDord-bcb59a40a1fc42e68225740f882fa5a6
Source noteuspto-grants-2015_08