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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912264Generated: October 27, 2026

(2,3,4-Trimethoxy-6-methylphenyl)(5-chloro-2-methoxy-4-methyl-3-pyridyl)methanol → Pyriofenone

https://huagongshe.com/reaction/1912264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3,4-Trimethoxy-6-methylphenyl)(5-chloro-2-methoxy-4-methyl-3-pyridyl)methanolHCID 23082593—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
ProductPyriofenoneHCID 2308266391.7%

Reaction Steps

4 g of active manganese dioxide was added to a toluene 15 ml solution of 0.64 g (1.7 mmol) of (2,3,4-trimethoxy-6-methylphenyl)(5-chloro-2-methoxy-4-methyl-3-pyridyl)methanol, followed by stirring under reflux with heating for 1 hour. The reaction solution was subjected to filtration on the pad of celite, and the solvent was distilled off under reduced pressure to obtain 0.57 g (yield: 90%) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-5-chloro-2-methoxy-4-methylpyridine (melting point 94.5 to 95.5° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609150B2
Source datasetuspto-grants-2013_12
ORD IDord-a9c6f5c930c04c368d37a7b8745c70f8
Source noteuspto-grants-2013_12