Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromotoluene | HCID 11560 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloro-6-methylnicotinic acid | HCID 121724 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11053930 | HCID 11053930 | 52.1% |
Reaction Steps
Magnesium (4.82 g, 200 mmol) was added to a tetrahydrofuran (300 ml) solution of 3-bromotoluene (35.1 g, 200 mmol), and the mixture was stirred at room temperature. Since spontaneous exothermic reaction occurred, the stirring was continued until the exothermicity was ceased. The reaction solution was cooled to -40° C., mixed with 2-chloro-6-methylnicotinic acid (11.6 g, 68 mmol) and then stirred for 16 hours at room temperature. The reaction solution was mixed with saturated ammonium chloride aqueous solution and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, magnesium sulfate was removed by filtration and then the filtrate was concentrated under a reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 2-chloro-6-methyl-3-(3-methylbenzoyl)pyridine (8.70 g, 52%) as a pale yellow oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136810 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-894023bd3d4e4540a4ee07cdb672db17 |
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| Source note | uspto-grants-2000_10 |
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