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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958797Generated: November 3, 2026

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

https://huagongshe.com/reaction/1958797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Ethyl-4-hydroxy-5-methylbenzaldehydeHCID 23159210—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product4-Benzyloxy-3-ethyl-5-methylbenzaldehydeHCID 8663934883.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (34.9 g, 0.213 mol) in MeCN (350 mL), K2CO3 (58.7 g, 0.425 mol) and benzylbromide (36.4 g, 0.213 mol) is added. The mixture is stirred at 60° C. for 2 h before it is cooled to rt, diluted with water and extracted twice with EA. The org. extracts are washed with water and concentrated to give crude 4-benzyloxy-3-ethyl-5-methyl-benzaldehyde as an orange oil (45 g). 1H NMR (CDCl3): δ1.29 (t, J=7.5 Hz, 3H), 2.40 (s, 3H), 2.77 (q, J=7.8 Hz, 2H), 4.90 (s, 2H), 7.31-7.52 (m, 5H), 7.62 (d, J=1.5 Hz, 1H), 7.66 (d, J=1.8 Hz, 1H), 9.94 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410151B2
Source datasetuspto-grants-2013_04
ORD IDord-dcada21f880745a78ba3c16194d3e0ab
Source noteuspto-grants-2013_04