Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3,4-diethyl 1H-pyrazole-3,4-dicarboxylate | HCID 14505699 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium ethoxide | HCID 2723922 | — |
| Product | HCID 67041773 | HCID 67041773 | 31% |
Reaction Steps
Sodium ethanolate solution was freshly prepared by dissolving sodium (240 mg) in ethanol (30 ml). 2H-Pyrazole-3,4-dicarboxylic acid diethyl ester (800 mg, 3.77 mmol) was dissolved in this sodium ethanolate solution (11 ml) and stirred for 10 min (r.t.), before ethyl iodide (1.4 g, 9 mmol) was added dropwise. After the completion of the addition, the mixture was heated to reflux until all starting material was consumed (1 h). The solvent was then evaporated, the residue was taken up in ethyl acetate and washed (water). The organic layer was dried (Na2SO4), evaporated, and the title compound (280 mg, 31%) was isolated from the mixture by column chromatography (silica gel, heptane:ethyl acetate=100:0-60:40). (The regioisomeric 1-ethyl-1H-pyrazole-3,4-dicarboxylic acid diethyl ester can also be isolated, and can be distinguished from the desired product by NOE-1H-NMR.) MS (m/e)=241.1 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263584B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-c41b67037b9849dc9a0d43ee889fcf9e |
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| Source note | uspto-grants-2012_09 |
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