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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108632Generated: October 30, 2026

4-(Methoxymethoxy)benzaldehyde → (2,6-Dimethyl-4-triisopropylsilanyloxyphenyl)-(4-methoxymethoxyphenyl)methanol

https://huagongshe.com/reaction/2108632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Methoxymethoxy)benzaldehydeHCID 250074—
Reactant(4-Bromo-3,5-dimethyl-phenoxy)triisopropylsilaneHCID 22605990—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2,6-Dimethyl-4-triisopropylsilanyloxyphenyl)-(4-methoxymethoxyphenyl)methanolHCID 66642856—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (4-bromo-3,5-dimethyl-phenoxy)triisopropylsilane (8.0 g, 23.30 mmol) in THF (50 mL) was added a solution of n-butyllithium (2.5 M in THF, 90 mL) at −78° C. The heterogeneous mixture was stirred at −78° C. for 1 h A solution of 4-methoxymethoxy-benzaldehyde (3.09 g, 18.58 mmol) in THF (5 mL) was added and the mixture was stirred at −78° C. for 1 h then warmed up to r.t. The reaction was then diluted with ethyl acetate and water, the layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were dried (MgSO4), filtered and concentrated to afford crude (2,6-dimethyl-4-triisopropylsilanyloxyphenyl)-(4-methoxymethoxyphenyl)methanol. Carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514419B2
Source datasetuspto-grants-2009_04
ORD IDord-011c5a64867a4a29ba264c2be9072e29
Source noteuspto-grants-2009_04