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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353188Generated: October 26, 2026

4-Hydroxybenzaldehyde → Tert-butyl 2-(4-formylphenoxy)acetate

https://huagongshe.com/reaction/353188

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantPotassium tert-butoxideHCID 23665647—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 2-(4-formylphenoxy)acetateHCID 639902—

Reaction Steps

At room temperature, 31.60 g (281.48 mmol) of potassium tert-butoxide and 52.70 g (270.22 mmol) of tert-butyl bromoacetate are added to a solution of 27.50 g (225.18 mmol) of 4-hydroxybenzaldehyde in 200 ml of dioxane, and the mixture is heated at the boil overnight. 1 l of water is added, and the mixture is then extracted with diethyl ether, washed with 1 N sodium hydroxide solution, water and saturated sodium chloride solution and dried over magnesium sulphate, and the solvent is distilled off. Flash chromatography on silica gel (cyclohexane→cyclohexane/ethyl acetate 20:1→10:1→5:1) gives, after recrystallization from pentane, the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750236B2
Source datasetuspto-grants-2004_06
ORD IDord-1bf31d3027f3447fbfed9be119745728
Source noteuspto-grants-2004_06