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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860673Generated: October 27, 2026

Sodium Hydroxide → 3-[4-(Benzyloxy)-3-methoxyphenyl]-2,2-dimethylpropanal

https://huagongshe.com/reaction/1860673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-(Benzyloxy)-4-(chloromethyl)-2-methoxybenzeneHCID 297962—
CatalystTetrabutylammonium IodideHCID 67553—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product3-[4-(Benzyloxy)-3-methoxyphenyl]-2,2-dimethylpropanalHCID 18624184—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under argon, a mixture of sodium hydroxide (1.43 g, 35.85 mmol) and tetrabutylammonium iodide (0.30 g, 0.82 mmol) in 8 ml benzene and 2.8 ml H2O was heated at 70° C. to form a homogeneous mixture. A mixture of the product of Step 1 (8.05 g, 30.64 mmol) and isobutraaldehyde (2.95 g, 40.85 mmol) in 20 ml benzene was added to the above solution dropwise. The resulting reaction mixture was heated at 70-75° C. for 6 h. The product was extracted with ethyl acetate and washed with H2O. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, dried with MgSO4, and concentrated. The residue was purified by chromatography (on silica gel, ethyl acetate/hexane=1/9) to yield a colorless oil in 8.32 g. NMR spectra of the product were consistent for the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531494B1
Source datasetuspto-grants-2003_03
ORD IDord-1e490710f6cc49a1bc9e06fbd5f6b380
Source noteuspto-grants-2003_03