HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396574Generated: October 29, 2026
Dimethylformamide → Ethyl 2-chloro-6-methylnicotinate
https://huagongshe.com/reaction/2396574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Ethyl dichlorocyanoacetate | HCID 10997655 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 2-chloro-6-methylnicotinate | HCID 15574421 | 73% |
Reaction Steps
To a mixture of 20 mL of toluene, 0.5 g of potassium acetate, 0.7 ml of triethylamine, and 4.25 g (40 mmol) of ethyl cyanoacetate at 5° C. were added dropwise 7.28 g (40 mmol) of ethyl 2,2-dichlorocyanoacetate. The resulting mixture was stirred at 5° C. for 30 min., and methyl vinyl ketone (4.2 g, 60 mmol) was added via a syringe pump in 1 h. After stirring at room temperature for 6 hours, 6.2 mL (80 mmol) of DMF was added, followed by slow addition of PCl3 (11 g, 80 mmol). Anhydrous HCl gas was bubbled in for 10 min., while keeping the reaction temperature around 65° C. After being heated at 80° C. for 1 hour, the reaction mixture was cooled, quenched with aqueous ammonium hydroxide, extracted with toluene, washed with 5% NaHCO3, and dried over MgSO4. Distillation afforded 5.83 g of the title compound. (36% yield, 112°-15° C./0.2 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05493028 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-f52badfe0875446d9fac7f63d6c46dd0 |
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| Source note | uspto-grants-1996_02 |
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