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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442727Generated: October 30, 2026

2-(3-Bromo-alpha-hydroxybenzyl)-3-methoxymethoxypyridine 1-oxide → 2-(3-Bromobenzoyl)-3-methoxymethoxy pyridine 1-oxide

https://huagongshe.com/reaction/442727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Bromo-alpha-hydroxybenzyl)-3-methoxymethoxypyridine 1-oxideHCID 54223976—
CatalystHCID 178418406HCID 178418406—
SolventEthyl AcetateHCID 8857—
Product2-(3-Bromobenzoyl)-3-methoxymethoxy pyridine 1-oxideHCID 5446568994.2%

Reaction Steps

A suspension of 2-(3-bromo-α-hydroxybenzyl)-3-methoxymethoxypyridine 1-oxide (4.58 g) and activated manganese dioxide (13.1 g) in ethyl acetate (150 mL) was stirred overnight at room temperature. The reaction mixture was subjected to filtration, and the filtrate was concentrated under reduced pressure. The concentrate was purified by means of a silica gel column (ethyl acetate--hexane) to afford 2-(3-bromobenzoyl)-3-methoxymethoxy pyridine 1-oxide (4.29 g). Physical properties and spectrum data of the product are shown below:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891895
Source datasetuspto-grants-1999_04
ORD IDord-d13c71dc392b4491977924931e22e7da
Source noteuspto-grants-1999_04