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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341126Generated: October 26, 2026

Picolinic acid → 1,3-Bis(1,1-dimethylethyl) 2-(3-iodo-5-methylphenyl)propanedioate

https://huagongshe.com/reaction/341126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantCesium carbonateHCID 10796—
ReactantDi-tert-butyl malonateHCID 68324—
Reactant1,3-Diiodo-5-methylbenzeneHCID 15505782—
CatalystCopper iodideHCID 83717—
Solvent1,4-DioxaneHCID 31275—
Product1,3-Bis(1,1-dimethylethyl) 2-(3-iodo-5-methylphenyl)propanedioateHCID 6828217916.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

Copper iodide (332 mg, 1.74 mmol), cesium carbonate (5.6 g, 17.4 mmol), and picolinic acid (429 mg, 3.49 mmol) were added to a dried flask under a nitrogen atmosphere. A solution of 3,5-diiodotoluene (3 g, 8.7 mmol) in dioxane (10 mL) was added, followed by the addition of di-tert-butyl malonate (1.3 mL, 8.7 mmol). The atmosphere inside the flask was removed under vacuum and replaced with nitrogen gas; this process was repeated a total of three times. The reaction mixture was then heated to 80° C. and stirred for 24 hours. The reaction mixture was then cooled to room temperature, quenched with saturated aqueous ammonium chloride solution (50 mL), and extracted twice with diethyl ether (50 mL). The organic layers were combined, dried over MgSO4, and concentrated under reduced pressure. The resulting residue was purified by chromatography on silica gel eluted with ethyl acetate in hexanes to provide the title product as an orange oil (0.62 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895738B2
Source datasetuspto-grants-2014_11
ORD IDord-ede37bb8c27a4898a3ebfd9b5219c928
Source noteuspto-grants-2014_11