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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295094Generated: October 30, 2026

4-Hydroxybenzaldehyde → Ethyl 2-(4-formylphenoxy)-2-methylpropanoate

https://huagongshe.com/reaction/1295094

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
SolventAcetoneHCID 180—
ProductEthyl 2-(4-formylphenoxy)-2-methylpropanoateHCID 13134808—

Reaction Steps

To 4-hydroxybenzaldehyde (20 g, 0.164 mol) in acetone (300 mL) was added K2CO3 (34 g, 1.5 equiv.) and the reaction was stirred at room temperature during 30 minutes. Ethyl 2-bromo-2-methylpropionate (36.2 mL, 1.5 equiv.) was added dropwise and the mixture was heated under reflux during 3 hours. K2CO3 (34 g, 1.5 equiv.) and ethyl 2-bromo-2-methylpropionate (36.2 mL, 1.5 equiv.) were added and the mixture was heated under reflux during 16 hours and then pourred into water and extracted with CH2Cl2 (3×300 mL). The combined organic layers were dried over Na2SO4, filtered and the solvent evaporated to afford crude intermediate. After chromatography on silicagel, eluting with cyclohexane/CH2Cl2 (6/4, then 8/2) and then with CH2Cl2, the titled compound was obtained as an oil (27 g, 69.85%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241793B2
Source datasetuspto-grants-2007_07
ORD IDord-3d53c01b911442af836b89f1d30140ed
Source noteuspto-grants-2007_07