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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175940Generated: October 31, 2026

Water → Methyl 2-methoxy-6-(pyrimidin-2-yl)benzoate

https://huagongshe.com/reaction/2175940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-BromopyrimidineHCID 78345—
ReactantMethyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 56776719—
CatalystHCID 178454861HCID 178454861—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-methoxy-6-(pyrimidin-2-yl)benzoateHCID 9041195163.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a microwave vial was dissolved methyl 2-methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (500 mg, 1.71 mmol), commercially available from Combi-Blocks (CAS #1146214-77-8), and 2-bromopyrimidine (344 mg, 2.05 mmol) in THF (8.5 mL). Na2CO3 (544 mg, 5.14 mmol) was then added followed by water (4 mL) and the reaction mixture was degassed with N2 for 10 minutes. PdCl2(dtbpf) (45 mg, 0.069 mmol) was then added and the reaction mixture was heated at 80° C. for 4 h. The mixture was cooled to room temperature and water and EtOAc added. The reaction mixture was extracted with EtOAc (3×). The combined organic layers were dried over Na2SO4, filtered, and concentrated. The crude was purified via silica gel chromatography (0-70% EtOAc in hexanes) to afford the title compound (265 mg, 63%). MS (ESI) mass calcd. for C13H12N2O3, 244.1; m/z found 245.1 [M+H]+. 1H NMR (400 MHz, Chloroform-d) 8.78 (d, J=4.9 Hz, 2H), 7.99 (dd, J=7.9, 0.9 Hz, 1H), 7.49 (t, J=8.1 Hz, 1H), 7.19 (t, J=4.8 Hz, 1H), 7.09 (dd, J=8.3, 0.9 Hz, 1H), 3.90 (s, 3H), 3.89 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062078B2
Source datasetuspto-grants-2015_06
ORD IDord-4c2338daf6ba4e78807337f637807b27
Source noteuspto-grants-2015_06