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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069119Generated: October 27, 2026

4-(Bromomethyl)benzyl alcohol → 4-(Bromomethyl)benzaldehyde

https://huagongshe.com/reaction/1069119

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)benzyl alcoholHCID 10330434—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product4-(Bromomethyl)benzaldehydeHCID 1120642157.3%

Reaction Steps

The 4-bromomethylbenzyl alcohol (9.0 g, 43 mmol) was reduced to the corresponding aldehyde by dissolving the above-synthesized intermediate in methylene chloride and then adding pyridinium chlorochromate (14.1 g, 6.5 mmol). The reaction mixture was then allowed to stir at room temperature under a nitrogen atmosphere for about oone hour. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was then filtered through a CELITE® pad, concentrated in vacuo, and then partitioned between equal volumes of diethyl ether and water. The organic fraction was washed with water, then with brine, and dried over magnesium sulfate. The solvents were removed in vacuo to yield a white crystalline solid. Recrystallization from hot diethyl ether yielded 4.9 grams of 4-(bromomethyl)benzaldehyde as needle-like crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251928B1
Source datasetuspto-grants-2001_06
ORD IDord-3f7c01d5f63d416fa7a062c7a1ce2c39
Source noteuspto-grants-2001_06