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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221143Generated: October 26, 2026

Toluene → Ethyl 3-(6-methylpyridin-2-yl)-3-oxopropanoate

https://huagongshe.com/reaction/2221143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl AcetateHCID 8857—
ReactantMethyl 6-methylpyridine-2-carboxylateHCID 73022—
ReactantSodium ethoxideHCID 2723922—
SolventAcetic AcidHCID 176—
ProductEthyl 3-(6-methylpyridin-2-yl)-3-oxopropanoateHCID 59710028112.6%

Reaction Conditions

Temperature92 °C

Reaction Steps

Stir a mixture of sodium ethoxide (90 g, 1.32 mol), toluene (0.5 L), and ethyl acetate (0.2 L, 1.98 mol) in a 2 L flask equipped with reflux condenser, mechanical stirrer, and nitrogen inlet. After 1 h, add 6-methyl-pyridine-2-carboxylic acid methyl ester (Cheung, Y, Tetrahedron Lett. 1979, 40, 3809-10; 100 g, 0.66 mol). Heat the mixture at reflux (92° C.) for 20 h. Cool the mixture to room temperature and acidify with glacial acetic acid to pH 6. Wash the resulting gel with water (0.5 L). Separate the layers and extract the aqueous layer with toluene (1×0.5 L) Dry the combined organic layers (sodium sulfate), filter, and concentrate in vacuo to yield the subtitled product (154 g) as a dark oil in 86% purity by HPLC analysis. MS ES+ m/e 208 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368445B2
Source datasetuspto-grants-2008_05
ORD IDord-2bc53a1bbaef4a4382476263a6a4ed57
Source noteuspto-grants-2008_05