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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240552Generated: October 31, 2026

Potassium Carbonate → Tert-butyl 4-(2-methyl-4-nitrophenoxy)pyridin-2-ylcarbamate

https://huagongshe.com/reaction/240552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
ReactantHCID 178452896HCID 178452896—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(2-methyl-4-nitrophenoxy)pyridin-2-ylcarbamateHCID 6693734030%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of tert-butyl 4-hydroxypyridin-2-ylcarbamate (4.12 g, 19.6 mmol) and 1-fluoro-2-methyl-4-nitrobenzene (3.34 g, 21.6 mmol) in DMF (40 mL) was added K2CO3 (4.06 g, 29.04 mmol). After heating to 65° C. for 64 hours, the mixture was cooled to room temperature and poured into ice water (200 mL). The reaction mixture was extracted several times with ethyl acetate. The combined organics were concentrated under reduced pressure. The residue was chromatographed (20% ethyl acetate in hexanes) to provide the product (2.03 g, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648087B2
Source datasetuspto-grants-2014_02
ORD IDord-78620a617fd748c29ce9748025b19eeb
Source noteuspto-grants-2014_02