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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800501Generated: October 26, 2026

Potassium Carbonate → Tert-butyl {4-methyl-3-[(5-nitropyridin-2-yl)oxy]phenyl}carbamate

https://huagongshe.com/reaction/1800501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactanttert-butyl N-(3-hydroxy-4-methylphenyl)carbamateHCID 44668374—
SolventDimethylformamideHCID 6228—
ProductTert-butyl {4-methyl-3-[(5-nitropyridin-2-yl)oxy]phenyl}carbamateHCID 8664600992%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-chloro-5-nitropyridine (15.0 g, 94.5 mmol) and tert-butyl (3-hydroxy-4-methylphenyl)carbamate (20.0 g, 90.0 mmol) in N,N-dimethylformamide (200 mL) was added potassium carbonate (18.6 g, 135 mmol), and the mixture was stirred at 70° C. for 18 hr. The reaction mixture was cooled to room temperature, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. Water (400 mL) was added to the obtained residue, and the mixture was extracted with ethyl acetate (400 mL×2). The combined organic layer was washed with saturated brine (300 mL×2), and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (ethyl acetate), and the obtained solution was concentrated under reduced pressure. The residue was triturated with hexane to give the title compound (28.6 g, 92%) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-e2a642f07ff14b37939311d23f3f2b8b
Source noteuspto-grants-2013_01