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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243769Generated: October 27, 2026

(2,3,4-Trimethoxy-6-methylphenyl)(5-bromo-4-chloro-2-methoxy-3-pyridyl)methanol → 3-(2,3,4-Trimethoxy-6-methylbenzoyl)-5-bromo-4-chloro-2-methoxypyridine

https://huagongshe.com/reaction/243769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3,4-Trimethoxy-6-methylphenyl)(5-bromo-4-chloro-2-methoxy-3-pyridyl)methanolHCID 23082647—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
Product3-(2,3,4-Trimethoxy-6-methylbenzoyl)-5-bromo-4-chloro-2-methoxypyridineHCID 1126268587%

Reaction Steps

4.55 g of manganese dioxide (88%, 46 mmol) was added to a solution having 2.21 g (5.1 mmol) of (2,3,4-trimethoxy-6-methylphenyl)(5-bromo-4-chloro-2-methoxy-3-pyridyl)methanol dissolved in 70 ml of toluene, followed by reflux with heating for 1 hour. 4.55 g of manganese dioxide (88%, 46 mmol) was further added, followed by reflux with heating for 1 hours. The reaction mixture was cooled to room temperature, manganese dioxide was removed by filtration on the pad of celite, and toluene was distilled off under reduced pressure. The obtained crude product was purified by silica gel chromatography to obtain 1.90 g (yield: 87%) of 3-(2,3,4-trimethoxy-6-methylbenzoyl)-5-bromo-4-chloro-2-methoxypyridine (melting point 84 to 87° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653277B2
Source datasetuspto-grants-2014_02
ORD IDord-c72d574868434ab6bf059f7578377838
Source noteuspto-grants-2014_02