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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835420Generated: November 3, 2026

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

https://huagongshe.com/reaction/1835420

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 to 4 ml of toluene and 8 ml of dimethylformamide at 0° C., followed by stirring for 10 minutes, and 4.0 g (10 mmol) of 4-(2,3,4-trimethoxy-6-methylbenzoyl)-3-methoxy-5-trifluoromethylpyridine-N-oxide was added thereto, followed by stirring for 20 minutes. Stirring was carried out at room temperature for 2 hours, and then the reaction solution was poured 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 thus obtained 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 (compound No. 123; m.p. 117-119° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770662B2
Source datasetuspto-grants-2004_08
ORD IDord-46bb9b8d05514d8c893e70c7d20db125
Source noteuspto-grants-2004_08