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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046233Generated: October 27, 2026

Sodium Thiosulfate → 3,5-diethyl 4-iodo-1H-pyrazole-3,5-dicarboxylate

https://huagongshe.com/reaction/2046233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
Reactantdiethyl 1H-pyrazole-3,5-dicarboxylateHCID 142184—
SolventChloroformHCID 6212—
Product3,5-diethyl 4-iodo-1H-pyrazole-3,5-dicarboxylateHCID 11739230104.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-iodosuccinimide (0.6 g, 2.59 mmol) was added to a solution of diethyl 3,5-pyrazoledicarboxylate (0.5 g, 2.35 mmol) in CHCl3 (10 mL) and the mixture was stirred at 80° C. for 24 hours. Then more of N-iodosuccinimide (0.6 g, 2.59 mmol) was added and the mixture was stirred at 100° C. for 48 hours more. Then the mixture was stirred at room temperature for 5 days. Then the mixture was treated with a saturated solution of Na2S2O3 and extracted with DCM. The organic layer was separated, dried (MgSO4), filtered and the solvents evaporated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH in DCM 0/100 to 10/90). The desired fractions were collected and the solvents evaporated in vacuo to yield 4-iodo-1H-pyrazole-3,5-dicarboxylic acid diethyl ester (0.83 g, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592422B2
Source datasetuspto-grants-2013_11
ORD IDord-5f1c0013b8b94e13916015598f68d070
Source noteuspto-grants-2013_11