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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849871Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 86703757, compound

https://huagongshe.com/reaction/1849871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantCyclopropylboronic acidHCID 2760897—
ReactantTri(cyclohexyl)phosphine tetrafluoroborateHCID 20066521—
ReactantHCID 86703756HCID 86703756—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 86703757HCID 8670375767%

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of tert-butyl 4-butoxy-5-chloro-2-fluorobenzoate (0.23 g, 0.76 mmol), cyclopropylboronic acid (0.10 g, 1.14 mmol), potassium phosphate (0.64 g, 3.10 mmol) and tricyclohexylphosphine tetrafluoroborate (0.05 g, 0.15 mmol) in toluene (3 mL) and water (0.3 mL) under a nitrogen atmosphere was added palladium acetate (0.005 g, 0.076 mmol). The reaction mixture was heated at 130° C. for 30 minutes in the microwave then cooled to ambient temperature. Water (20 mL) was added and the mixture extracted with ethyl acetate (2×15 mL). The combined organics were washed with brine; dried over anhydrous sodium sulfate and concentrated in vacuo. Purification of the residue by column chromatography (5% ethyl acetate in hexanes) afforded tert-butyl 4-butoxy-5-cyclopropyl-2-fluorobenzoate (0.15 g, 67%), which was used directly in the next step. To a solution of this compound (0.15 g, 0.48 mmol) in dichloromethane (2 mL), was added trifluoroacetic acid (2 mL). The reaction mixture was stirred at room temperature for 1 hour and then concentrated in vacuo. The residue was triturated in diethyl ether (10 mL) and the solid was filtered, rinsed with diethyl ether (2×10 mL) and dried to give the title compound (0.048 g, 40%). 1H NMR (300 MHz, CDCl3) δ 7.48 (d, J=8.3 Hz, 1H), 6.56 (d, J=12.7 Hz, 1H), 4.08-3.95 (m, 2H), 2.18-0.39 (m, 14H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-d0c8ad3a84034661b888aa5c232fa968
Source noteuspto-grants-2015_02