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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771452Generated: October 26, 2026

Potassium Carbonate → 3-Fluoro-4-(6-hydroxynaphthalen-2-yl)benzoic acid

https://huagongshe.com/reaction/1771452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-2-naphthalenolHCID 27144—
Reactant2-Fluoro-4-(methoxycarbonyl)benzeneboronic acidHCID 24824345—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-Fluoro-4-(6-hydroxynaphthalen-2-yl)benzoic acidHCID 5738640375.1%

Reaction Steps

6-Bromonaphthalen-2-ol (1 g, 4.48 mmol) was mixed with 880 mg of 2-fluoro-4-(methoxycarbonyl)phenylboronic acid (4.48 mmol), 1.2 g of K2CO3 (9.23 mmol), 120 mg of Pd(PPh3)4 (2.5 mol %), and then suspended in 17 mL of 1,4-Dioxane and 4 mL of H2O. The mixture was degassed 3× with argon and then heated to reflux while stirring for 1 hour. 4N NaOH (5 mL) was then added and stirred at room temperature for 2 hours, back extracted with EtOAc, and filtered through Celite. The basic aqueous solution was then acidified to pH=4.3 and the solids were filtered to give about 950 mg of off-white solid. This was triturated in 8 mL DCM and 2 mL EtOAc and filtered to yield about 830 mg of off-white Example 2 (65.8% overall yield). 1H-NMR (DMSO-d6 500 MHz): δ 13.31 (bs, 1H), 9.97 (bs, 1H), 8.05 (s, 1H), 7.90 (m, 2H), 7.80 (m, 3H), 7.64 (dt, 1H), 7.19 (m, 2H); MS (ESI): m/z 281.53 [MA]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249132B2
Source datasetuspto-grants-2016_02
ORD IDord-8c738ed9021d4facad4e0820d977d500
Source noteuspto-grants-2016_02