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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242302Generated: November 2, 2026

Sodium Iodide → HCID 87258798, compound

https://huagongshe.com/reaction/1242302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant3-Chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridineHCID 21935751—
ReactantHCID 67072166HCID 67072166—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 87258798HCID 87258798—

Reaction Steps

To 0.080 g (0.29 mmol) of the above prepared (4-methylamino-2-trifluoromethyl-phenoxy)-acetic acid ethyl ester and 0.124 g (0.43 mmol) of 3-chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine (see example 1N], dissolved in 1.0 ml of abs. DMSO, were added successively 0.048 g (0.32 mmol) of NaI and 0.066 g (0.43 mmol) of DBU. The reaction was allowed to proceed for 4 h at ambient temperature, when TLC still indicated some starting amine. Therefore, another 33 mg (0.4 eq.) of 3-chloromethyl-2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine was added and stirring continued for 3 h. Pouring onto crashed ice, extraction with AcOEt, filtration over Celite, washing of the organic layer with water, drying over sodium sulfate, and evaporation of the solvents, followed by flash chromatography (SiO2, hexane/AcOEt=8/2), afforded 0.046 g of the title compound as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-7f32f42372a7414c9a72a07e89e0cc67
Source noteuspto-grants-2006_10