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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantCyclopropanecarboxylic acidHCID 15655—
ReactantAmmonium PersulfateHCID 62648—
ReactantEthyl 2,4-dimethylnicotinateHCID 736245—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product6-Cyclopropyl-2,4-dimethyl-nicotinic acid ethyl esterHCID 6877683318%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790747B2
Source datasetuspto-grants-2010_09
ORD IDord-dd77f1aa9d69488f91bcb34894fc3b18
Source noteuspto-grants-2010_09