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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108635Generated: October 30, 2026

Tetrabutylammonium Fluoride → 5-(4-Hydroxy-2,6-dimethylbenzyl)-2-methoxymethoxybenzaldehyde

https://huagongshe.com/reaction/2108635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-(2,6-Dimethyl-4-triisopropylsilanyloxybenzyl)-2-methoxymethoxybenzaldehydeHCID 86603457—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-(4-Hydroxy-2,6-dimethylbenzyl)-2-methoxymethoxybenzaldehydeHCID 8660345864%

Reaction Steps

To a solution of 5-(2,6-dimethyl-4-triisopropylsilanyloxybenzyl)-2-methoxymethoxy-benzaldehyde (1.4 g, 3.07 mmol) in THF (15 mL) was added TBAF (1 M, 3.68 mL) at 0° C. After stirring at r.t. for 2 h, the reaction mixture was diluted with EtOAc and water. The water layer was extracted with EtOAc and the combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate-hexanes; 1:9) to afford 5-(4-hydroxy-2,6-dimethylbenzyl)-2-methoxymethoxybenzaldehyde (590 mg, 64% for two steps): 1H NMR (200 MHz, CDCl3): δ 10.45 (s, 1H), 7.54 (s, 1H), 7.27 (m, 1H), 7.09 (m, 1H), 6.56(s, 2H), 5.25 (s, 2H), 3.92 (s, 2H), 3.50 (s, 3H), 2.16 (s, 6H). TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=ethyl acetate-hexanes (1:9); Rf=0.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514419B2
Source datasetuspto-grants-2009_04
ORD IDord-b6d15837304c434eb257db6493dbb59d
Source noteuspto-grants-2009_04