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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666588Generated: November 1, 2026

Benzyl Bromide → 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde

https://huagongshe.com/reaction/1666588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Ethyl-4-hydroxy-5-methylbenzaldehydeHCID 23159210—
SolventAcetoneHCID 180—
Product4-Benzyloxy-3-ethyl-5-methylbenzaldehydeHCID 8663934873.2%

Reaction Steps

To a solution of 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (8.00 g, 48.7 mmol) in acetone (130 mL), K2CO3 (20.2 g, 146.2 mmol) followed by benzylbromide (12.5 g, 73.1 mmol) is added. The suspension is stirred at reflux for 16 h before it is filtered and the solvent of the filtrate is removed in vacuo. The residue is separated by CC on silica gel to give 4-benzyloxy-3-ethyl-5-methyl-benzaldehyde (9.07 g) as a pale yellow oil; LC-MS: tR=1.09 min, [M+1]+=255.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044076B2
Source datasetuspto-grants-2011_10
ORD IDord-9227861861ea4721af7554b752c562fa
Source noteuspto-grants-2011_10