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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247768Generated: November 1, 2026

(4-Bromo-2-methylphenyl)methanol → 4-Bromo-2-methylbenzaldehyde

https://huagongshe.com/reaction/2247768

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Bromo-2-methylphenyl)methanolHCID 22280088—
ReactantMethyl 1-({5-[5-(3-fluoro-4-phenoxyphenyl)-1,2,4-oxadiazol-3-yl]-4-methyl-2-thienyl}methyl)azetidine-3-carboxylateHCID 68525875—
Product4-Bromo-2-methylbenzaldehydeHCID 13555150—

Reaction Steps

The crude product of the title compound was synthesized by conducting the reaction similar to that mentioned in Example 24 (24f) using (4-bromo-2-methylphenyl)methanol (3.7 g, 19 mmol) that was obtained in Example 27 (27a) and pyridinium dichromate (11g, 28 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:19 to 1:4) as the eluent to afford the title compound (2.4 g) in a yield of 64% as a colourless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-dd78867db45b4fce8df324a5a013e0dd
Source noteuspto-grants-2010_03