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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912252Generated: October 26, 2026

4,5-Dichloro-2-methoxy-alpha-(2,3,4-trimethoxy-6-methylphenyl)-3-pyridinemethanol → (4,5-Dichloro-2-methoxy-3-pyridinyl)(2,3,4-trimethoxy-6-methylphenyl)methanone

https://huagongshe.com/reaction/1912252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,5-Dichloro-2-methoxy-alpha-(2,3,4-trimethoxy-6-methylphenyl)-3-pyridinemethanolHCID 23082608—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product(4,5-Dichloro-2-methoxy-3-pyridinyl)(2,3,4-trimethoxy-6-methylphenyl)methanoneHCID 2308266065%

Reaction Steps

13.8 g (159 mmol) of manganese dioxide was added to a solution having 4.66 g (12.0 mmol) of (2,3,4-trimethoxy-6-methylphenyl)(4,5-dichloro-2-methoxy-3-pyridyl)methanol obtained in Step (f) dissolved in 30 ml of toluene, followed by reflux with heating for 2 hours. After cooling to room temperature, manganese dioxide was removed by filtration on the pad of celite, and toluene was distilled off under reduced pressure, followed by purification by silica gel column chromatography to obtain 2.98 g (yield: 65%) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-4,5-dichloro-2-methoxypyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609150B2
Source datasetuspto-grants-2013_12
ORD IDord-d9ac9c530183476882aa8b8c005146f6
Source noteuspto-grants-2013_12