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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | tert-butyl N-(3-hydroxy-4-methylphenyl)carbamate | HCID 44668374 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl {4-methyl-3-[(5-nitropyridin-2-yl)oxy]phenyl}carbamate | HCID 86646009 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344135B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-e2a642f07ff14b37939311d23f3f2b8b |
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| Source note | uspto-grants-2013_01 |
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