HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711154Generated: October 26, 2026
Ammonium Hydroxide → 6-Cyclopropyl-2,4-dimethyl-nicotinic acid ethyl ester
https://huagongshe.com/reaction/1711154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Cyclopropanecarboxylic acid | HCID 15655 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Reactant | Ethyl 2,4-dimethylnicotinate | HCID 736245 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 6-Cyclopropyl-2,4-dimethyl-nicotinic acid ethyl ester | HCID 68776833 | 18% |
Reaction Steps
To a solution of ethyl 2,4-dimethylpyridine-3-carboxylate (0.59 g, 3.29 mmol) and cyclopropane carboxylic acid (1.2 ml (15.1 mmol) in 10% aqueous H2SO4 (3 ml) was added AgNO3 (154 mg, 0.91 mmol) followed by a solution of ammonium persulfate (1:541 g, 6.75 mmol) in water (6 ml) and the mixture stirred at room temperature overnight. The reaction was neutralized to pH 10 with saturated aqueous NH4OH (5 ml) and extracted with EtOAc (3×20 ml). The combined organic extracts were dried (Na2SO4), concentrated and purified by column chromatography on silica gel (Hexanes/EtOAc, 96:4 then 1:1 then 0:100) to afford desired 6-cyclopropyl-2,4-dimethyl-nicotinic acid ethyl ester (133 mg, 18%) as a clear oil along with recovered starting ethyl 2,4-dimethylpyridine-3-carboxylate (0.31 g). 1H NMR (CDCl3) δ 0.93-0.97 (m, 4H), 1.38 (t, 3H, J=6 Hz), 1.92-2.02 (m, 1H), 2.28 (s, 3H), 2.47 (s, 3H), 4.39 (q, 2H, J=6 Hz), 6.73 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790747B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-dd77f1aa9d69488f91bcb34894fc3b18 |
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| Source note | uspto-grants-2010_09 |
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