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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958328Generated: October 26, 2026

Iodoethane → HCID 67041773, compound

https://huagongshe.com/reaction/1958328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodiumHCID 5360545—
Reactant3,4-diethyl 1H-pyrazole-3,4-dicarboxylateHCID 14505699—
SolventEthanolHCID 702—
SolventSodium ethoxideHCID 2723922—
ProductHCID 67041773HCID 6704177331%

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 at RT, 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-'H-NMR.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410117B2
Source datasetuspto-grants-2013_04
ORD IDord-1671379c5ebc48a79efb1b0b3351954a
Source noteuspto-grants-2013_04