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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835401Generated: October 31, 2026

(2,3,4-Trimethoxy-6-methylphenyl)(2,5-dichloro-3-trifluoromethyl-4-pyridyl)methanol → 2,3,4-Trimethoxy-6-methylbenzoyl-2,5-dichloro-3-trifluoromethylpyridine

https://huagongshe.com/reaction/1835401

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3,4-Trimethoxy-6-methylphenyl)(2,5-dichloro-3-trifluoromethyl-4-pyridyl)methanolHCID 12151535—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product2,3,4-Trimethoxy-6-methylbenzoyl-2,5-dichloro-3-trifluoromethylpyridineHCID 1215153689%

Reaction Steps

14 g of manganese dioxide was added to a solution having 3.5 g (8.2 mmol) of (2,3,4-trimethoxy-6-methylphenyl)(2,915 5-dichloro-3-trifluoromethyl-4-pyridyl)methanol obtained in step (b) dissolved in 100 ml of toluene, followed by stirring under reflux by heating for 6 hours. The mixture was cooled and then subjected to filtration, and toluene was distilled off under reduced pressure. The crude product thus obtained was purified by silica gel column chromatography to obtain 3.1 g (yield 89%) of 4-(2,3,4-trimethoxy-6-methylbenzoyl-2,5-dichloro-3-trifluoromethylpyridine (compound No. 90; m.p. 106-109° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770662B2
Source datasetuspto-grants-2004_08
ORD IDord-13c53c5717f743b1ab35d8eaae8f35d4
Source noteuspto-grants-2004_08