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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427000Generated: November 4, 2026

Methyl 4-bromobenzoate → HCID 22730763, compound

https://huagongshe.com/reaction/1427000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-bromobenzoateHCID 12081—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 22730763HCID 2273076396.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

Toluene (20 mL), ethanol (6 mL), and water (2 mL) were added to commercially available 1-N—BOC-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,6-dihydro-2H-pyridine (1.00 g, 3.23 mmol), methyl 4-bromobenzoate (695 mg, 3.23 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy biphenyl (266 mg, 0.65 mmol), palladium(II) acetate (73 mg, 0.32 mmol), and tripotassium phosphate (2.06 g, 9.70 mmol) under nitrogen atmosphere, and the mixture was stirred at 90° C. for 5 hours. The reaction mixture was cooled to room temperature and a saturated aqueous sodium bicarbonate solution and ethyl acetate were added for partition. The aqueous layer was extracted with ethyl acetate three times and then the organic layer was dried over anhydrous sodium sulfate and filtered. The solvent was evaporated and the resultant residue was purified with silica gel column chromatography (n-heptane:ethyl acetate=19:1-13:7) to obtain the title compound (0.99 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933099B2
Source datasetuspto-grants-2015_01
ORD IDord-2ec424bbd8e84c82b376f7a6194b340a
Source noteuspto-grants-2015_01