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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13446Generated: October 26, 2026

Potassium Carbonate → Tert-butyl 4-(4-amino-3-nitrophenoxy)picolinate

https://huagongshe.com/reaction/13446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant4-Amino-3-NitrophenolHCID 3758882—
Reactanttert-Butyl 4-chloropicolinateHCID 11806045—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(4-amino-3-nitrophenoxy)picolinateHCID 22041090—

Reaction Conditions

Temperature80 °C

Reaction Steps

Solid anhydrous white powdered KHMDS (2 eq) was suspended in a solution of dimethylformamide. Red crystalline 4-amino-3-nitrophenol (1 eq) was charged to the rapidly stirring solution under an inert atmosphere and the heterogeneous solution was allowed to stir for 2 hours. Then a dimethylformamide solution of tert-butyl 4-chloropyridine-2-carboxylate (1 eq) was added dropwise. Anhydrous powdered potassium carbonate (1.2 eq) was charged to the reaction as an acid scavenger. The purple colored viscous mixture was heated to 80° C. for 12-15 hours until when it was determined to be complete by HPLC. The reaction was evaporated under reduced pressure and diluted with excess ethyl acetate and water. An extraction of the aqueous layer was made with ethyl acetate. The organic layers were combined and washed 4 times with water followed by brine. The organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure. The crude material was purified by flash silica gel chromatography using an eluent of 1:1 mixture of hexanes to ethyl acetate to give the desired product. MS: MH+=332.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728010B2
Source datasetuspto-grants-2010_06
ORD IDord-00d13c5c1a234708ab4cef80b7b55f27
Source noteuspto-grants-2010_06