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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351817Generated: October 26, 2026

4-Hydroxybenzaldehyde → 4-Isopropoxybenzaldehyde

https://huagongshe.com/reaction/351817

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product4-IsopropoxybenzaldehydeHCID 25007777.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2 g (16.38 mmol) of 4-hydroxybenzaldehyde in 100 mL of DMF, 2.72 g (19.69 mmol) of K2CO3, 2.74 g (16.52 mmol) of KI and 3.94 mL (39.38 mmol) of 2-iodopropane was added under argon. The mixture was stirred at 80° C. overnight, concentrated and the residue obtained was partitioned between CHCl3 and H2O. The phases were separated, the aqueous phase was extracted with CHCl3 and the combined organic phases were dried over MgSO4 and concentrated. The crude product obtained was purified by chromatography on silica gel using EtOAc/hexane mixtures of increasing polarity as eluent, to give 2.08 g of the title compound of the example as an oil (77% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743816B2
Source datasetuspto-grants-2004_06
ORD IDord-894b4acbbcc04531b679f4df06420873
Source noteuspto-grants-2004_06