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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874350Generated: October 25, 2026

Dimethylformamide → Tert-butyl {4-methyl-3-[(6-nitropyridin-3-yl)oxy]phenyl}carbamate

https://huagongshe.com/reaction/1874350

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant5-Bromo-2-nitropyridineHCID 817620—
Reactanttert-butyl N-(3-hydroxy-4-methylphenyl)carbamateHCID 44668374—
SolventWaterHCID 962—
ProductTert-butyl {4-methyl-3-[(6-nitropyridin-3-yl)oxy]phenyl}carbamateHCID 5774914546%

Reaction Steps

A mixture of tert-butyl (3-hydroxy-4-methylphenyl)carbamate (3.14 g, 14.1 mmol), 5-bromo-2-nitropyridine (2.38 g, 11.7 mmol), cesium carbonate (5.72 g, 17.6 mmol) and N,N-dimethylformamide (25 mL) was stirred at room temperature for 15 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (NH silica gel, hexane/ethyl acetate=80/20→0/100) to give the title compound (1.86 g, 44%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-9874cd7a11d7454a8e441d5e4e888b0e
Source noteuspto-grants-2012_11