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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242419Generated: October 26, 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/242419

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 numberUS08653113B2
Source datasetuspto-grants-2014_02
ORD IDord-05644f751d854b8aadc22a7f849016d8
Source noteuspto-grants-2014_02