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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541037Generated: October 31, 2026

Toluene → 4,5,6-Trichloropicolinoyl chloride

https://huagongshe.com/reaction/541037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Pyridinecarboxylic acid, 4,5,6-trichloro-HCID 12993692—
SolventDimethylformamideHCID 6228—
Product4,5,6-Trichloropicolinoyl chlorideHCID 12993693117.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

A 500 mL three neck round bottom flask with thermowell was fitted with a condenser which vented to a trap and then an aqueous 10% NaOH scrubber, magnetic stir bar, two stoppers and a thermometer. To the vessel was added 4,5,6-trichloropicolinic acid (86 g which contained 8.6 g water, 77.4 g active, 0.32 mol), toluene (160 mL), thionyl chloride (85 mL, 1.12 mol) and DMF (0.3 mL). The slurry was heated to 70-80° C., held there for 7 h and then cooled to room temperature and allowed to stir overnight. Approximately 0.2 mL of the pale yellow solution was placed in a vial and concentrated to a solid under a stream of N2. The solid was treated with a mixture of triethylamine/methanol (0.3 mL/2 mL) and then warmed with a heat gun for ca. 1 min. HPLC analysis indicated that less than 1% of the carboxylic acid remained as compared to the methyl ester derivative. The solution was concentrated on a rotary evaporator leaving a pale yellow solid. The solid was dried (40° C./20 mmHg) for about 1 h providing the title compound (92 g): mp 68-70° C.; 1H NMR (CDCl3, 400 MHz) δ 8.12 (s), the solid contained about 4 wt % toluene as determined by integration of the proton signals; 13C NMR (CDCl3, 101 MHz) δ 167.3, 151.0, 145.82, 145.8, 135.7, 125.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871943B2
Source datasetuspto-grants-2014_10
ORD IDord-f8b8cedfc946405c89509b9ad71907b0
Source noteuspto-grants-2014_10