Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242436Generated: October 31, 2026

Toluene → 4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-chloro-3-trifluoromethyl-5-methoxypyridine

https://huagongshe.com/reaction/242436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine-N-oxideHCID 12151305—
SolventDimethylformamideHCID 6228—
Product4-(2,3,4-Trimethoxy-6-methylbenzoyl)-2-chloro-3-trifluoromethyl-5-methoxypyridineHCID 1215142285%

Reaction Steps

1.8 ml (19 mmol) of phosphorus oxychloride was added at 0° C. to 4 ml of toluene and 8 ml of dimethylformamide, followed by stirring for 10 minutes, and then 4.0 g (10 mmol) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine-N-oxide was added, followed by stirring for 20 minutes. After stirring at room temperature for 2 hours, the reaction solution was charged into ice water to terminate the reaction. The aqueous layer was extracted with ethyl acetate, and then the organic layer was dried over anhydrous sodium sulfate and subjected to filtration, and the solvent was distilled off under reduced pressure. The crude product was purified by silica gel column chromatography to obtain 3.57 g (yield: 85%) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-2-chloro-3-trifluoromethyl-5-methoxypyridine (melting point 117 to 119° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653113B2
Source datasetuspto-grants-2014_02
ORD IDord-abba62824cc1492e89de2121748c2949
Source noteuspto-grants-2014_02