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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190496Generated: October 31, 2026

Potassium Carbonate → Tert-butyl [3-(3-amino-4-nitrophenoxy)phenyl]carbamate

https://huagongshe.com/reaction/2190496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-nitroanilineHCID 75399—
Reactanttert-butyl N-(3-hydroxyphenyl)carbamateHCID 312485—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl [3-(3-amino-4-nitrophenoxy)phenyl]carbamateHCID 8665540969%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of tert-butyl (3-hydroxyphenyl)carbamate (6.89 g, 32.9 mmol) and 5-fluoro-2-nitroaniline (5.09 g, 32.6 mmol) in N,N-dimethylformamide (100 mL) was added potassium carbonate (11.2 g, 80.9 mmol), and the mixture was vigorously stirred at 100° C. for 14 hr. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (125 ml) and hexane (125 mL), washed with water (150 mL×2) and saturated brine (100 mL), successively, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (ethyl acetate/hexane=2/98→30/70) to give the title compound (7.7 g, 69%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324395B2
Source datasetuspto-grants-2012_12
ORD IDord-d7477199369342ce9c2a8186166303dd
Source noteuspto-grants-2012_12