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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541052Generated: October 31, 2026

Dimethylformamide → HCID 86709877, compound

https://huagongshe.com/reaction/541052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-DimethylaminopyridineHCID 21885—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 86709870HCID 86709870—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 86709877HCID 86709877—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 4,5-dichloro-6-(4-methoxyphenyl)-picolinic acid (4.50 g, 15.1 mmol) in toluene (40 mL) was added thionyl chloride (1.65 mL, 22.6 mmol) and dimethylformamide (0.06 mL, 0.8 mmol). Reaction mixture was heated at 80° C. for 12 h. HPLC analysis of an aliquot of the reaction mixture treated with methanol and dimethylaminopyridine indicated complete conversion of the starting material. Reaction mixture was allowed to cool to room temperature and concentrated under reduced pressure to provide a yellow solid. Toluene (40 mL) was added to dissolve the solid and concentrated under reduced pressure and then this process was performed a second time. 4,5-Dichloro-6-(4-methoxyphenyl)-picolinoyl chloride was isolated as a yellow solid (4.64 g, 97% yield). 1H NMR (400 MHz, CDCl3) δ 8.09 (s, 1H), 7.85-7.77 (m, 2H), 7.06-6.98 (m, 2H); 13C NMR (101 MHz, CDCl3) δ 168.91, 161.06, 158.35, 146.26, 145.13, 133.92, 131.35, 129.16, 124.13, 113.70; MS Calcd. for C13H8Cl3NO2: 314.96. Found: 253, 218.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871943B2
Source datasetuspto-grants-2014_10
ORD IDord-293e66d49aa646eb87a36eaa78995c7d
Source noteuspto-grants-2014_10