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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990111Generated: October 26, 2026

Benzyl Bromide → 4-(Benzyloxy)-3-nitrobenzaldehyde

https://huagongshe.com/reaction/990111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-3-nitrobenzaldehydeHCID 18169—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-3-nitrobenzaldehydeHCID 7023554—

Reaction Steps

Substituted benzyl bromide compounds can also be prepared from commercially available substituted benzaldehydes, benzoic acids and benzoic esters by first converting these compounds to the corresponding alcohol. Exemplary synthetic methodology to provide substituted benzyl bromide from benzyl aldehyde is described below. For example, as illustrated in Scheme 12, treatment of 4-hydroxy-3-nitro-benzaldehyde 73 with benzyl bromide in the presence of K2CO3 in DMF at 65° C. gives 4-benzyloxy-3-nitro-benzaldehyde 74. Reduction of compound 74 in methanol with NaBH4 affords the alcohol 75 and subsequent bromination using PBr3 in diethyl ether provides the desired bromide compound 76.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458829B1
Source datasetuspto-grants-2002_10
ORD IDord-0eaa3129489645d48cc52af19fec94cd
Source noteuspto-grants-2002_10