HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602544Generated: October 30, 2026
Water → 2-(2,6-Dimethyl-phenyl)4-methyl-5-nitro-pyridine
https://huagongshe.com/reaction/602544
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-4-methyl-5-nitropyridine | HCID 345364 | — |
| Reactant | 2,6-Dimethylphenylboronic acid | HCID 583322 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(2,6-Dimethyl-phenyl)4-methyl-5-nitro-pyridine | HCID 67152544 | — |
Reaction Steps
A mixture of 2,6-dimethylphenylboronic acid (6.5 g, 43.5 mmol), 2-chloro-4-methyl-5-nitro-pyridine (5 g, 28.9 mmol), Pd(PPh3)4, (1.5 g, 1.5 mmol), Na2CO3 (4.6 g, 43.5 mm water (20 mL), and EtOH (5 mL) is heated in a sealed tube under nitrogen at 110° C. for 18 hours. The mixture is cooled to room temperature, diluted with EtOAc (150 mL), washed with saturated solution of Na2CO3 (50 mL 3×), water (50 mL) and brine (50 mL), dried (Na2SO4), and concentrated under reduced pressure. The residue is purified by chromatography on silica gel (Hexane/EtOAc, 6:1) to afford 2-(2,6-dimethyl-phenyl)-4-methyl-5-nitro-pyridine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906528B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-8405865ab2ca428dac4aa38ec0ba3e14 |
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| Source note | uspto-grants-2011_03 |
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