HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751254Generated: October 26, 2026
Toluene → Ethyl 3-(6-methylpyridin-2-yl)-3-oxopropanoate
https://huagongshe.com/reaction/751254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methyl 6-methylpyridine-2-carboxylate | HCID 73022 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 3-(6-methylpyridin-2-yl)-3-oxopropanoate | HCID 59710028 | 112.6% |
Reaction Steps
Stir a mixture of sodium ethoxide (90 g, 1.32 mol, 2 eq), toluene (0.5 L, 5 vol), and ethyl acetate (0.2 L, 1.98 mol, 3 eq) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405299B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-9e7952648ad74ddc88db4efa9ed90fb9 |
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| Source note | uspto-grants-2008_07 |
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